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: 6 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 20 |
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: 3, no: 20 |
NetGPI | no | yes: 0, no: 23 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 21 |
GO:0110165 | cellular anatomical entity | 1 | 21 |
Related structures:
AlphaFold database: A4H8H6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 28 | 30 | PF00675 | 0.588 |
CLV_PCSK_SKI1_1 | 29 | 33 | PF00082 | 0.461 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.599 |
DOC_MAPK_MEF2A_6 | 5 | 13 | PF00069 | 0.507 |
DOC_USP7_MATH_1 | 124 | 128 | PF00917 | 0.233 |
DOC_USP7_MATH_1 | 199 | 203 | PF00917 | 0.694 |
DOC_USP7_MATH_1 | 207 | 211 | PF00917 | 0.671 |
DOC_WW_Pin1_4 | 151 | 156 | PF00397 | 0.268 |
DOC_WW_Pin1_4 | 203 | 208 | PF00397 | 0.651 |
LIG_14-3-3_CanoR_1 | 29 | 35 | PF00244 | 0.365 |
LIG_14-3-3_CanoR_1 | 39 | 43 | PF00244 | 0.302 |
LIG_BRCT_BRCA1_1 | 21 | 25 | PF00533 | 0.378 |
LIG_EH1_1 | 3 | 11 | PF00400 | 0.467 |
LIG_eIF4E_1 | 4 | 10 | PF01652 | 0.458 |
LIG_FHA_1 | 115 | 121 | PF00498 | 0.359 |
LIG_FHA_1 | 133 | 139 | PF00498 | 0.351 |
LIG_FHA_1 | 18 | 24 | PF00498 | 0.449 |
LIG_FHA_1 | 66 | 72 | PF00498 | 0.407 |
LIG_FHA_2 | 147 | 153 | PF00498 | 0.391 |
LIG_LIR_Gen_1 | 163 | 173 | PF02991 | 0.286 |
LIG_LIR_Nem_3 | 163 | 169 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 22 | 28 | PF02991 | 0.343 |
LIG_LIR_Nem_3 | 3 | 7 | PF02991 | 0.486 |
LIG_SH2_CRK | 4 | 8 | PF00017 | 0.406 |
LIG_SH2_PTP2 | 80 | 83 | PF00017 | 0.183 |
LIG_SH2_STAP1 | 139 | 143 | PF00017 | 0.365 |
LIG_SH2_STAP1 | 67 | 71 | PF00017 | 0.400 |
LIG_SH2_STAT5 | 137 | 140 | PF00017 | 0.310 |
LIG_SH2_STAT5 | 67 | 70 | PF00017 | 0.393 |
LIG_SH2_STAT5 | 80 | 83 | PF00017 | 0.276 |
LIG_SH3_3 | 142 | 148 | PF00018 | 0.350 |
LIG_SH3_3 | 201 | 207 | PF00018 | 0.786 |
LIG_SUMO_SIM_anti_2 | 127 | 133 | PF11976 | 0.326 |
LIG_SUMO_SIM_par_1 | 116 | 122 | PF11976 | 0.241 |
LIG_SUMO_SIM_par_1 | 8 | 14 | PF11976 | 0.375 |
LIG_TYR_ITIM | 2 | 7 | PF00017 | 0.450 |
LIG_TYR_ITIM | 78 | 83 | PF00017 | 0.228 |
LIG_UBA3_1 | 23 | 30 | PF00899 | 0.456 |
LIG_WRC_WIRS_1 | 12 | 17 | PF05994 | 0.191 |
LIG_WRC_WIRS_1 | 120 | 125 | PF05994 | 0.318 |
MOD_CDC14_SPxK_1 | 154 | 157 | PF00782 | 0.266 |
MOD_CDK_SPxK_1 | 151 | 157 | PF00069 | 0.272 |
MOD_CK1_1 | 210 | 216 | PF00069 | 0.633 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.392 |
MOD_CK1_1 | 84 | 90 | PF00069 | 0.324 |
MOD_CK2_1 | 146 | 152 | PF00069 | 0.290 |
MOD_CK2_1 | 55 | 61 | PF00069 | 0.497 |
MOD_GlcNHglycan | 126 | 129 | PF01048 | 0.294 |
MOD_GlcNHglycan | 209 | 212 | PF01048 | 0.599 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.651 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.386 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.432 |
MOD_GSK3_1 | 114 | 121 | PF00069 | 0.360 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.371 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.353 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.701 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.672 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.366 |
MOD_N-GLC_1 | 109 | 114 | PF02516 | 0.394 |
MOD_N-GLC_1 | 50 | 55 | PF02516 | 0.620 |
MOD_NEK2_1 | 11 | 16 | PF00069 | 0.358 |
MOD_NEK2_1 | 118 | 123 | PF00069 | 0.344 |
MOD_NEK2_1 | 19 | 24 | PF00069 | 0.317 |
MOD_NEK2_1 | 217 | 222 | PF00069 | 0.712 |
MOD_NEK2_2 | 38 | 43 | PF00069 | 0.285 |
MOD_PKA_1 | 29 | 35 | PF00069 | 0.338 |
MOD_PKA_2 | 38 | 44 | PF00069 | 0.428 |
MOD_Plk_1 | 109 | 115 | PF00069 | 0.593 |
MOD_Plk_1 | 215 | 221 | PF00069 | 0.583 |
MOD_Plk_4 | 114 | 120 | PF00069 | 0.405 |
MOD_Plk_4 | 133 | 139 | PF00069 | 0.264 |
MOD_Plk_4 | 19 | 25 | PF00069 | 0.400 |
MOD_ProDKin_1 | 151 | 157 | PF00069 | 0.272 |
MOD_ProDKin_1 | 203 | 209 | PF00069 | 0.652 |
TRG_DiLeu_BaEn_1 | 164 | 169 | PF01217 | 0.310 |
TRG_ENDOCYTIC_2 | 4 | 7 | PF00928 | 0.463 |
TRG_ENDOCYTIC_2 | 80 | 83 | PF00928 | 0.311 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3Z4 | Leptomonas seymouri | 31% | 100% |
A0A0N0P3Z6 | Leptomonas seymouri | 39% | 98% |
A0A0N0P4D5 | Leptomonas seymouri | 40% | 100% |
A0A0N1HU04 | Leptomonas seymouri | 28% | 71% |
A0A0N1PD13 | Leptomonas seymouri | 26% | 95% |
A0A1X0P9D7 | Trypanosomatidae | 24% | 100% |
A0A3Q8IIZ2 | Leishmania donovani | 46% | 100% |
A0A3R7KFR8 | Trypanosoma rangeli | 31% | 100% |
A0A3S5H6X1 | Leishmania donovani | 37% | 100% |
A0A3S7WTU4 | Leishmania donovani | 31% | 100% |
A4H8H3 | Leishmania braziliensis | 31% | 98% |
A4H8H5 | Leishmania braziliensis | 35% | 100% |
A4HWU5 | Leishmania infantum | 31% | 100% |
A4HWU7 | Leishmania infantum | 37% | 100% |
A4HWU8 | Leishmania infantum | 46% | 100% |
C9ZMZ8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
E9AQK5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
E9AQK7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 39% | 100% |
E9AQK8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 43% | 100% |
Q4QEX0 | Leishmania major | 44% | 100% |
Q4QEX1 | Leishmania major | 38% | 100% |
Q4QEX3 | Leishmania major | 32% | 99% |