Similar to reticulons (structural ER membrane proteins) of multicellular animals.. The toplology is difficult to assess, likely owing to the fact that these proteins are curvature-inducing. Localization: ER (by homology)
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 15 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005783 | endoplasmic reticulum | 5 | 2 |
GO:0005789 | endoplasmic reticulum membrane | 4 | 11 |
GO:0016020 | membrane | 2 | 11 |
GO:0031090 | organelle membrane | 3 | 11 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
Related structures:
AlphaFold database: Q4Q737
Term | Name | Level | Count |
---|---|---|---|
GO:0009605 | response to external stimulus | 2 | 10 |
GO:0009607 | response to biotic stimulus | 2 | 10 |
GO:0009617 | response to bacterium | 3 | 10 |
GO:0043207 | response to external biotic stimulus | 3 | 10 |
GO:0044419 | biological process involved in interspecies interaction between organisms | 1 | 10 |
GO:0050896 | response to stimulus | 1 | 10 |
GO:0051707 | response to other organism | 2 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 193 | 195 | PF00675 | 0.497 |
CLV_PCSK_KEX2_1 | 68 | 70 | PF00082 | 0.374 |
CLV_PCSK_PC1ET2_1 | 68 | 70 | PF00082 | 0.374 |
CLV_PCSK_SKI1_1 | 6 | 10 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 76 | 80 | PF00082 | 0.231 |
DEG_MDM2_SWIB_1 | 32 | 40 | PF02201 | 0.414 |
DOC_MAPK_gen_1 | 68 | 74 | PF00069 | 0.597 |
DOC_PP4_FxxP_1 | 143 | 146 | PF00568 | 0.347 |
DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.548 |
DOC_USP7_MATH_1 | 85 | 89 | PF00917 | 0.576 |
LIG_14-3-3_CanoR_1 | 21 | 29 | PF00244 | 0.539 |
LIG_14-3-3_CanoR_1 | 69 | 75 | PF00244 | 0.528 |
LIG_APCC_ABBA_1 | 38 | 43 | PF00400 | 0.492 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.672 |
LIG_BRCT_BRCA1_1 | 111 | 115 | PF00533 | 0.446 |
LIG_BRCT_BRCA1_1 | 29 | 33 | PF00533 | 0.375 |
LIG_EH1_1 | 114 | 122 | PF00400 | 0.446 |
LIG_FHA_1 | 11 | 17 | PF00498 | 0.514 |
LIG_FHA_1 | 116 | 122 | PF00498 | 0.385 |
LIG_FHA_1 | 131 | 137 | PF00498 | 0.316 |
LIG_FHA_1 | 142 | 148 | PF00498 | 0.298 |
LIG_FHA_1 | 45 | 51 | PF00498 | 0.452 |
LIG_FHA_1 | 92 | 98 | PF00498 | 0.560 |
LIG_FHA_2 | 10 | 16 | PF00498 | 0.622 |
LIG_FHA_2 | 103 | 109 | PF00498 | 0.535 |
LIG_FHA_2 | 174 | 180 | PF00498 | 0.595 |
LIG_LIR_Apic_2 | 18 | 22 | PF02991 | 0.564 |
LIG_LIR_Gen_1 | 34 | 44 | PF02991 | 0.392 |
LIG_LIR_Gen_1 | 83 | 93 | PF02991 | 0.574 |
LIG_LIR_Nem_3 | 105 | 109 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 30 | 35 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 7 | 11 | PF02991 | 0.631 |
LIG_LIR_Nem_3 | 83 | 89 | PF02991 | 0.545 |
LIG_MLH1_MIPbox_1 | 29 | 33 | PF16413 | 0.375 |
LIG_Pex14_2 | 124 | 128 | PF04695 | 0.428 |
LIG_Pex14_2 | 29 | 33 | PF04695 | 0.425 |
LIG_SH2_STAP1 | 109 | 113 | PF00017 | 0.604 |
LIG_SH2_STAP1 | 166 | 170 | PF00017 | 0.611 |
LIG_SH2_STAT5 | 170 | 173 | PF00017 | 0.615 |
LIG_SH2_STAT5 | 44 | 47 | PF00017 | 0.297 |
LIG_SH3_3 | 69 | 75 | PF00018 | 0.597 |
LIG_SUMO_SIM_anti_2 | 130 | 138 | PF11976 | 0.374 |
LIG_SUMO_SIM_anti_2 | 55 | 60 | PF11976 | 0.492 |
LIG_SUMO_SIM_par_1 | 98 | 105 | PF11976 | 0.555 |
LIG_WRC_WIRS_1 | 29 | 34 | PF05994 | 0.375 |
LIG_WRC_WIRS_1 | 46 | 51 | PF05994 | 0.367 |
MOD_CK1_1 | 130 | 136 | PF00069 | 0.346 |
MOD_CK1_1 | 180 | 186 | PF00069 | 0.672 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.423 |
MOD_CK1_1 | 99 | 105 | PF00069 | 0.525 |
MOD_CK2_1 | 173 | 179 | PF00069 | 0.633 |
MOD_CK2_1 | 180 | 186 | PF00069 | 0.612 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.525 |
MOD_GlcNHglycan | 111 | 114 | PF01048 | 0.367 |
MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.370 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.670 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.428 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.374 |
MOD_NEK2_1 | 115 | 120 | PF00069 | 0.439 |
MOD_NEK2_1 | 129 | 134 | PF00069 | 0.277 |
MOD_NEK2_1 | 173 | 178 | PF00069 | 0.650 |
MOD_NEK2_1 | 96 | 101 | PF00069 | 0.502 |
MOD_NEK2_2 | 85 | 90 | PF00069 | 0.542 |
MOD_PK_1 | 181 | 187 | PF00069 | 0.659 |
MOD_PK_1 | 52 | 58 | PF00069 | 0.492 |
MOD_PKA_1 | 181 | 187 | PF00069 | 0.714 |
MOD_Plk_1 | 130 | 136 | PF00069 | 0.345 |
MOD_Plk_1 | 42 | 48 | PF00069 | 0.384 |
MOD_Plk_1 | 97 | 103 | PF00069 | 0.574 |
MOD_Plk_4 | 116 | 122 | PF00069 | 0.353 |
MOD_Plk_4 | 130 | 136 | PF00069 | 0.288 |
MOD_Plk_4 | 28 | 34 | PF00069 | 0.374 |
MOD_Plk_4 | 45 | 51 | PF00069 | 0.417 |
MOD_Plk_4 | 52 | 58 | PF00069 | 0.365 |
MOD_SUMO_rev_2 | 191 | 196 | PF00179 | 0.718 |
MOD_SUMO_rev_2 | 2 | 11 | PF00179 | 0.714 |
TRG_ENDOCYTIC_2 | 170 | 173 | PF00928 | 0.664 |
TRG_ENDOCYTIC_2 | 86 | 89 | PF00928 | 0.554 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P527 | Leptomonas seymouri | 56% | 100% |
A0A0S4JFE7 | Bodo saltans | 31% | 100% |
A0A1X0P1J2 | Trypanosomatidae | 36% | 100% |
A0A3Q8IFS1 | Leishmania donovani | 93% | 100% |
A0A3R7L2P9 | Trypanosoma rangeli | 34% | 100% |
A4HII9 | Leishmania braziliensis | 74% | 100% |
C9ZR54 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
E9B128 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
Q28D16 | Xenopus tropicalis | 21% | 92% |
Q9NJS2 | Leishmania infantum | 93% | 100% |