Descriptions

The autoinhibited protein was predicted that may have potential autoinhibitory elements via cis-regPred.

Autoinhibitory domains (AIDs)

Target domain

Relief mechanism

Assay

cis-regPred

Accessory elements

No accessory elements

Autoinhibited structure

Activated structure

1 structures for A7YY97

Entry ID Method Resolution Chain Position Source
AF-A7YY97-F1 Predicted AlphaFoldDB

No variants for A7YY97

Variant ID(s) Position Change Description Diseaes Association Provenance
No variants for A7YY97

1 associated diseases with A7YY97

[MIM: 615500]: Ciliary dyskinesia, primary, 26 (CILD26)

A disorder characterized by abnormalities of motile cilia. Respiratory infections leading to chronic inflammation and bronchiectasis are recurrent, due to defects in the respiratory cilia. Patients may exhibit randomization of left-right body asymmetry and situs inversus, due to dysfunction of monocilia at the embryonic node. Primary ciliary dyskinesia associated with situs inversus is referred to as Kartagener syndrome. {ECO:0000269|PubMed:24094744}. Note=The disease is caused by variants affecting the gene represented in this entry. Cilia in nasal epithelia show the absence of both outer and inner dynein-arm components and complete paralysis.

Without disease ID
  • A disorder characterized by abnormalities of motile cilia. Respiratory infections leading to chronic inflammation and bronchiectasis are recurrent, due to defects in the respiratory cilia. Patients may exhibit randomization of left-right body asymmetry and situs inversus, due to dysfunction of monocilia at the embryonic node. Primary ciliary dyskinesia associated with situs inversus is referred to as Kartagener syndrome. {ECO:0000269|PubMed:24094744}. Note=The disease is caused by variants affecting the gene represented in this entry. Cilia in nasal epithelia show the absence of both outer and inner dynein-arm components and complete paralysis.

No regional properties for A7YY97

Type Name Position InterPro Accession
No domain, repeats, and functional sites for A7YY97

Functions

Description
EC Number
Subcellular Localization
  • Cytoplasm
PANTHER Family
PANTHER Subfamily
PANTHER Protein Class
PANTHER Pathway Category No pathway information available

1 GO annotations of cellular component

Name Definition
cytoplasm The contents of a cell excluding the plasma membrane and nucleus, but including other subcellular structures.

3 GO annotations of molecular function

Name Definition
chaperone binding Binding to a chaperone protein, a class of proteins that bind to nascent or unfolded polypeptides and ensure correct folding or transport.
heat shock protein binding Binding to a heat shock protein, a protein synthesized or activated in response to heat shock.
unfolded protein binding Binding to an unfolded protein.

2 GO annotations of biological process

Name Definition
protein folding The process of assisting in the covalent and noncovalent assembly of single chain polypeptides or multisubunit complexes into the correct tertiary structure.
protein stabilization Any process involved in maintaining the structure and integrity of a protein and preventing it from degradation or aggregation.

6 homologous proteins in AiPD

UniProt AC Gene Name Protein Name Species Evidence Code
P06101 CDC37 Hsp90 co-chaperone Cdc37 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) (Baker's yeast) PR
Q5EAC6 CDC37 Hsp90 co-chaperone Cdc37 Bos taurus (Bovine) PR
Q24276 Cdc37 Hsp90 co-chaperone Cdc37 Drosophila melanogaster (Fruit fly) PR
Q16543 CDC37 Hsp90 co-chaperone Cdc37 Homo sapiens (Human) PR
Q61081 Cdc37 Hsp90 co-chaperone Cdc37 Mus musculus (Mouse) PR
Q63692 Cdc37 Hsp90 co-chaperone Cdc37 Rattus norvegicus (Rat) PR
10 20 30 40 50 60
MASLCQRQQH CVKASIASEW QLAEAQDQLC GLELHSSESV EQERARALAS STELSHTEHQ
70 80 90 100 110 120
WRLKERMLGT LCPEANRDVF DKSIINITQS WPNESDPDKS LNFVQRNEEL LKHFGMLGRW
130 140 150 160 170 180
DDSQRFLAEY HHLICEETAN YLILWCFRLQ AEKKEALMEQ VAHQAVVMQF ILEMARNTQQ
190 200 210 220 230 240
DPRGCFRHFF QKAKAGQEGY LDVFHTELQA FKDRVKEYTM KSTGETPKDT VHQNTPPACC
250 260 270 280 290 300
LDPKEVFESL PQELKTCIQM QDMQILQNVL SSMNPQVAEY HVKRCLEAGL WTNIPRTSKD
310
ESSEVDEWKM MET