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FLAD1 and ANXA7
Number of citations of the paper that reports this interaction (PMID
21900206
)
27
Data Source:
BioGRID
(two hybrid)
FLAD1
ANXA7
Gene Name
flavin adenine dinucleotide synthetase 1
annexin A7
Image
No pdb structure
No pdb structure
Gene Ontology Annotations
Cellular Component
Cytoplasm
Mitochondrial Matrix
Cytosol
Plasma Membrane
Nucleus
Nuclear Envelope
Endoplasmic Reticulum Membrane
Cytosol
Plasma Membrane
Membrane
Chromaffin Granule Membrane
Extracellular Vesicular Exosome
Molecular Function
FMN Adenylyltransferase Activity
ATP Binding
Integrin Binding
Calcium Ion Binding
Protein Binding
Calcium-dependent Phospholipid Binding
Poly(A) RNA Binding
Calcium-dependent Protein Binding
Biological Process
FAD Biosynthetic Process
Vitamin Metabolic Process
Water-soluble Vitamin Metabolic Process
Riboflavin Metabolic Process
Mo-molybdopterin Cofactor Biosynthetic Process
Small Molecule Metabolic Process
Cellular Calcium Ion Homeostasis
Autophagy
Hemostasis
Cell Proliferation
Regulation Of Cell Shape
Response To Salt Stress
Cellular Water Homeostasis
Negative Regulation Of Gene Expression
Response To Organic Cyclic Compound
Epithelial Cell Differentiation
Social Behavior
Response To Calcium Ion
Membrane Fusion
Pathways
Metabolism of vitamins and cofactors
Defective CD320 causes methylmalonic aciduria
Defective GIF causes intrinsic factor deficiency
Defective LMBRD1 causes methylmalonic aciduria and homocystinuria type cblF
Defective HLCS causes multiple carboxylase deficiency
Defective MMAB causes methylmalonic aciduria type cblB
Defective BTD causes biotidinase deficiency
Defective MMACHC causes methylmalonic aciduria and homocystinuria type cblC
Defective MMADHC causes methylmalonic aciduria and homocystinuria type cblD
Defective MTR causes methylmalonic aciduria and homocystinuria type cblG
Defective MTRR causes methylmalonic aciduria and homocystinuria type cblE
Defective MMAA causes methylmalonic aciduria type cblA
Vitamin B2 (riboflavin) metabolism
Defective CUBN causes hereditary megaloblastic anemia 1
Defective AMN causes hereditary megaloblastic anemia 1
Metabolism of water-soluble vitamins and cofactors
Defective MUT causes methylmalonic aciduria mut type
Defects in biotin (Btn) metabolism
Defective TCN2 causes hereditary megaloblastic anemia
Defects in vitamin and cofactor metabolism
Defects in cobalamin (B12) metabolism
Drugs
Diseases
GWAS
Prostate cancer (
23535732
)
Protein-Protein Interactions
13 interactors:
ANXA7
CDKN1A
GEMIN4
GRB7
NUDT21
PRTFDC1
RCC1
REL
SDCBP
SMN1
TCF4
TK1
TRIM23
108 interactors:
A1BG
A2M
ACTB
ACTL6B
ADAMTS10
ANGPT2
APC
APLP1
ATP5B
ATP6V1A
ATXN3
BAG6
C14orf1
CCDC90B
CCT7
CDK4
CELF3
CENPB
CHGB
CLEC3B
COL11A2
COL4A2
COL4A5
COPS6
CPNE2
CPNE6
CPSF3L
CRMP1
CSAD
CTSB
DDAH2
DMPK
DOCK7
DVL1
DYNC1I1
EEF1A1
EXT2
F13A1
FAF1
FBN3
FGB
FLAD1
GAPDH
GBP2
GDF9
GNB2
GNB5
HADHB
HMGXB3
HOXD8
INPP5K
KLHL23
KMT2B
LRIF1
MED31
MPPED1
MSH2
NGFR
NMT2
NPRL2
OTUB1
PAAF1
PAX8
PDCD6
PDHB
PKM
PLD3
PRKACA
PRKCA
PRKCB
PRKCG
PRKG1
PSMB10
QARS
RBBP4
RBM48
RPA1
RPL13
RPS2
S100A10
SDF4
SEMA5B
SETDB1
SMPD1
SP110
SRC
SRI
SUMO3
TAF5L
TIAM2
TLE1
TMEM108
TMSB4X
TP53
TRMT2A
TUBA1A
TUBB2B
TUBB3
UBE2D1
UCHL5
UNC119
USP4
VIM
WDR18
WDR73
ZBTB16
ZNF135
ZNF431
Entrez ID
80308
310
HPRD ID
17887
01720
Ensembl ID
ENSG00000160688
ENSG00000138279
Uniprot IDs
Q8NFF5
B2R657
P20073
PDB IDs
Enriched GO Terms of Interacting Partners
?
Cellular Component Assembly
Digestive Tract Development
Digestive System Development
Ribonucleoprotein Complex Assembly
MRNA Splicing, Via Spliceosome
RNA Splicing, Via Transesterification Reactions
Cellular Macromolecular Complex Assembly
Spliceosomal SnRNP Assembly
Negative Regulation Of Gene Expression
Ribonucleoprotein Complex Biogenesis
Fetal Process Involved In Parturition
RNA Splicing
Skeletal Muscle Cell Proliferation
Catenin Import Into Nucleus
Canonical Wnt Signaling Pathway Involved In Positive Regulation Of Epithelial To Mesenchymal Transition
MRNA Processing
Protein Tetramerization
Response To Extracellular Stimulus
Positive Regulation Of Heparan Sulfate Proteoglycan Biosynthetic Process
Regulation Of Cellular Component Organization
Positive Regulation Of Extracellular Vesicular Exosome Assembly
Maintenance Of DNA Repeat Elements
MRNA Metabolic Process
Cell Cycle Arrest
Intestinal Epithelial Cell Maturation
RNA Processing
Positive Regulation Of Signal Transduction
Response To Glucocorticoid
G1/S Transition Of Mitotic Cell Cycle
Regulation Of Extracellular Vesicular Exosome Assembly
Negative Regulation Of Type B Pancreatic Cell Apoptotic Process
Response To Cortisol
Thymidine Metabolic Process
Embryonic Hindgut Morphogenesis
Epidermal Growth Factor Receptor Signaling Pathway
ERBB Signaling Pathway
Response To Corticosteroid
Small GTPase Mediated Signal Transduction
Embryonic Genitalia Morphogenesis
Response To Toxic Substance
Positive Regulation Of Metabolic Process
Deoxyribonucleoside Monophosphate Biosynthetic Process
Cellular Response To UV-B
Myoblast Fate Commitment
Transmembrane Receptor Protein Tyrosine Kinase Signaling Pathway
Positive Regulation Of Ran GTPase Activity
Tube Development
Secretory Granule Localization
Pyrimidine Nucleoside Salvage
Pyrimidine-containing Compound Salvage
Anatomical Structure Development
Multicellular Organismal Development
Developmental Process
System Development
Cellular Metabolic Process
Metabolic Process
Cellular Response To Organic Substance
Platelet Activation
Regulation Of Protein Metabolic Process
Regulation Of Metabolic Process
Cellular Response To Growth Factor Stimulus
Regulation Of Cellular Protein Metabolic Process
Blood Coagulation
Response To Growth Factor
Programmed Cell Death
Hemostasis
Negative Regulation Of Cellular Protein Metabolic Process
Cell Death
Catabolic Process
Death
Response To Organic Substance
Apoptotic Process
Histone H3-T6 Phosphorylation
Regulation Of Apoptotic Process
Nervous System Development
Regulation Of Body Fluid Levels
Negative Regulation Of Protein Metabolic Process
Regulation Of Cell Death
Negative Regulation Of Cellular Metabolic Process
Regulation Of Protein Catabolic Process
Cellular Protein Metabolic Process
Regulation Of Proteolysis
Mitotic Cell Cycle Process
Negative Regulation Of Glucose Transport
Organelle Organization
Cell Activation
Enzyme Linked Receptor Protein Signaling Pathway
Regulation Of Catalytic Activity
Cellular Process
Regulation Of Cellular Response To Insulin Stimulus
Wound Healing
Cellular Response To Stimulus
Regulation Of Proteasomal Protein Catabolic Process
Gene Expression
Protein Metabolic Process
Mitotic Cell Cycle
Organ Development
Biosynthetic Process
Cellular Nitrogen Compound Metabolic Process
Chromosome Organization
Tagcloud
?
annexin
anticancer
antitumor
chinese
cytotoxic
cytotoxicity
decreasing
depressed
dramatically
eecp
ethanol
exerted
explored
huvecs
kappa
mb
mcf
mda
mitochondrial
mu
obviously
p65
possess
propolis
ros
umbilical
upregulating
vein
Tagcloud (Difference)
?
annexin
anticancer
antitumor
chinese
cytotoxic
cytotoxicity
decreasing
depressed
dramatically
eecp
ethanol
exerted
explored
huvecs
kappa
mb
mcf
mda
mitochondrial
mu
obviously
p65
possess
propolis
ros
umbilical
upregulating
vein
Tagcloud (Intersection)
?