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. | no | yes: 0 |
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: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: E9AIE5
Term | Name | Level | Count |
---|---|---|---|
GO:0000413 | protein peptidyl-prolyl isomerization | 7 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0018193 | peptidyl-amino acid modification | 5 | 12 |
GO:0018208 | peptidyl-proline modification | 6 | 12 |
GO:0019538 | protein metabolic process | 3 | 12 |
GO:0036211 | protein modification process | 4 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043412 | macromolecule modification | 4 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003755 | peptidyl-prolyl cis-trans isomerase activity | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0016853 | isomerase activity | 2 | 12 |
GO:0016859 | cis-trans isomerase activity | 3 | 12 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 266 | 270 | PF00656 | 0.610 |
CLV_C14_Caspase3-7 | 282 | 286 | PF00656 | 0.505 |
CLV_C14_Caspase3-7 | 63 | 67 | PF00656 | 0.337 |
CLV_NRD_NRD_1 | 163 | 165 | PF00675 | 0.492 |
CLV_NRD_NRD_1 | 258 | 260 | PF00675 | 0.752 |
CLV_NRD_NRD_1 | 317 | 319 | PF00675 | 0.669 |
CLV_NRD_NRD_1 | 430 | 432 | PF00675 | 0.516 |
CLV_PCSK_FUR_1 | 255 | 259 | PF00082 | 0.755 |
CLV_PCSK_KEX2_1 | 163 | 165 | PF00082 | 0.581 |
CLV_PCSK_KEX2_1 | 183 | 185 | PF00082 | 0.555 |
CLV_PCSK_KEX2_1 | 242 | 244 | PF00082 | 0.667 |
CLV_PCSK_KEX2_1 | 257 | 259 | PF00082 | 0.744 |
CLV_PCSK_KEX2_1 | 315 | 317 | PF00082 | 0.596 |
CLV_PCSK_KEX2_1 | 430 | 432 | PF00082 | 0.637 |
CLV_PCSK_PC1ET2_1 | 183 | 185 | PF00082 | 0.575 |
CLV_PCSK_PC1ET2_1 | 242 | 244 | PF00082 | 0.575 |
CLV_PCSK_PC1ET2_1 | 315 | 317 | PF00082 | 0.596 |
CLV_PCSK_SKI1_1 | 303 | 307 | PF00082 | 0.650 |
CLV_PCSK_SKI1_1 | 98 | 102 | PF00082 | 0.405 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.384 |
DEG_SPOP_SBC_1 | 392 | 396 | PF00917 | 0.725 |
DEG_SPOP_SBC_1 | 61 | 65 | PF00917 | 0.326 |
DOC_CKS1_1 | 157 | 162 | PF01111 | 0.578 |
DOC_CYCLIN_yCln2_LP_2 | 43 | 49 | PF00134 | 0.535 |
DOC_MAPK_gen_1 | 28 | 37 | PF00069 | 0.381 |
DOC_MAPK_gen_1 | 83 | 92 | PF00069 | 0.397 |
DOC_PP2B_LxvP_1 | 140 | 143 | PF13499 | 0.565 |
DOC_PP2B_LxvP_1 | 43 | 46 | PF13499 | 0.525 |
DOC_PP4_FxxP_1 | 20 | 23 | PF00568 | 0.394 |
DOC_USP7_MATH_1 | 125 | 129 | PF00917 | 0.523 |
DOC_USP7_MATH_1 | 222 | 226 | PF00917 | 0.728 |
DOC_USP7_MATH_1 | 273 | 277 | PF00917 | 0.673 |
DOC_USP7_MATH_1 | 288 | 292 | PF00917 | 0.760 |
DOC_USP7_MATH_1 | 390 | 394 | PF00917 | 0.714 |
DOC_USP7_MATH_1 | 413 | 417 | PF00917 | 0.724 |
DOC_USP7_MATH_2 | 232 | 238 | PF00917 | 0.550 |
DOC_USP7_UBL2_3 | 380 | 384 | PF12436 | 0.457 |
DOC_USP7_UBL2_3 | 421 | 425 | PF12436 | 0.778 |
DOC_WW_Pin1_4 | 156 | 161 | PF00397 | 0.546 |
DOC_WW_Pin1_4 | 309 | 314 | PF00397 | 0.506 |
LIG_14-3-3_CanoR_1 | 184 | 193 | PF00244 | 0.583 |
LIG_14-3-3_CanoR_1 | 28 | 33 | PF00244 | 0.387 |
LIG_14-3-3_CanoR_1 | 296 | 302 | PF00244 | 0.473 |
LIG_14-3-3_CanoR_1 | 333 | 339 | PF00244 | 0.703 |
LIG_Actin_WH2_2 | 168 | 185 | PF00022 | 0.541 |
LIG_BIR_III_2 | 285 | 289 | PF00653 | 0.538 |
LIG_BRCT_BRCA1_1 | 290 | 294 | PF00533 | 0.694 |
LIG_BRCT_BRCA1_1 | 297 | 301 | PF00533 | 0.635 |
LIG_BRCT_BRCA1_1 | 5 | 9 | PF00533 | 0.473 |
LIG_FHA_1 | 174 | 180 | PF00498 | 0.458 |
LIG_FHA_1 | 332 | 338 | PF00498 | 0.631 |
LIG_FHA_1 | 85 | 91 | PF00498 | 0.414 |
LIG_FHA_1 | 95 | 101 | PF00498 | 0.379 |
LIG_FHA_2 | 10 | 16 | PF00498 | 0.313 |
LIG_FHA_2 | 156 | 162 | PF00498 | 0.552 |
LIG_FHA_2 | 270 | 276 | PF00498 | 0.752 |
LIG_FHA_2 | 54 | 60 | PF00498 | 0.532 |
LIG_FHA_2 | 61 | 67 | PF00498 | 0.497 |
LIG_LIR_Apic_2 | 19 | 23 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 134 | 140 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 165 | 169 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 19 | 24 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 212 | 216 | PF02991 | 0.616 |
LIG_LIR_Nem_3 | 99 | 104 | PF02991 | 0.395 |
LIG_PTB_Apo_2 | 31 | 38 | PF02174 | 0.343 |
LIG_REV1ctd_RIR_1 | 292 | 300 | PF16727 | 0.711 |
LIG_REV1ctd_RIR_1 | 352 | 360 | PF16727 | 0.634 |
LIG_SH2_CRK | 137 | 141 | PF00017 | 0.532 |
LIG_SH2_CRK | 213 | 217 | PF00017 | 0.485 |
LIG_SH2_PTP2 | 151 | 154 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 151 | 154 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 62 | 65 | PF00017 | 0.323 |
LIG_SH3_1 | 242 | 248 | PF00018 | 0.710 |
LIG_SH3_3 | 103 | 109 | PF00018 | 0.431 |
LIG_SH3_3 | 154 | 160 | PF00018 | 0.503 |
LIG_SH3_3 | 242 | 248 | PF00018 | 0.710 |
LIG_SUMO_SIM_anti_2 | 4 | 9 | PF11976 | 0.390 |
LIG_SUMO_SIM_par_1 | 87 | 97 | PF11976 | 0.412 |
LIG_TYR_ITIM | 135 | 140 | PF00017 | 0.512 |
LIG_TYR_ITIM | 211 | 216 | PF00017 | 0.603 |
MOD_CDC14_SPxK_1 | 312 | 315 | PF00782 | 0.506 |
MOD_CDK_SPxK_1 | 309 | 315 | PF00069 | 0.507 |
MOD_CDK_SPxxK_3 | 156 | 163 | PF00069 | 0.478 |
MOD_CDK_SPxxK_3 | 309 | 316 | PF00069 | 0.505 |
MOD_CK1_1 | 156 | 162 | PF00069 | 0.421 |
MOD_CK1_1 | 345 | 351 | PF00069 | 0.457 |
MOD_CK1_1 | 393 | 399 | PF00069 | 0.707 |
MOD_CK1_1 | 408 | 414 | PF00069 | 0.532 |
MOD_CK1_1 | 416 | 422 | PF00069 | 0.656 |
MOD_CK1_1 | 94 | 100 | PF00069 | 0.398 |
MOD_CK2_1 | 155 | 161 | PF00069 | 0.516 |
MOD_CK2_1 | 215 | 221 | PF00069 | 0.533 |
MOD_CK2_1 | 269 | 275 | PF00069 | 0.568 |
MOD_CK2_1 | 53 | 59 | PF00069 | 0.501 |
MOD_CK2_1 | 85 | 91 | PF00069 | 0.499 |
MOD_CK2_1 | 9 | 15 | PF00069 | 0.497 |
MOD_Cter_Amidation | 240 | 243 | PF01082 | 0.782 |
MOD_Cter_Amidation | 381 | 384 | PF01082 | 0.439 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.434 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.767 |
MOD_GlcNHglycan | 281 | 284 | PF01048 | 0.666 |
MOD_GlcNHglycan | 297 | 300 | PF01048 | 0.602 |
MOD_GlcNHglycan | 307 | 310 | PF01048 | 0.727 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.499 |
MOD_GlcNHglycan | 408 | 411 | PF01048 | 0.738 |
MOD_GlcNHglycan | 422 | 425 | PF01048 | 0.771 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.423 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.544 |
MOD_GSK3_1 | 265 | 272 | PF00069 | 0.727 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.646 |
MOD_GSK3_1 | 413 | 420 | PF00069 | 0.683 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.387 |
MOD_N-GLC_1 | 279 | 284 | PF02516 | 0.726 |
MOD_NEK2_1 | 153 | 158 | PF00069 | 0.432 |
MOD_NEK2_1 | 174 | 179 | PF00069 | 0.452 |
MOD_NEK2_1 | 289 | 294 | PF00069 | 0.649 |
MOD_NEK2_1 | 295 | 300 | PF00069 | 0.556 |
MOD_NEK2_1 | 332 | 337 | PF00069 | 0.624 |
MOD_NEK2_1 | 37 | 42 | PF00069 | 0.392 |
MOD_NEK2_1 | 391 | 396 | PF00069 | 0.626 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.406 |
MOD_PIKK_1 | 142 | 148 | PF00454 | 0.509 |
MOD_PIKK_1 | 184 | 190 | PF00454 | 0.578 |
MOD_PIKK_1 | 234 | 240 | PF00454 | 0.690 |
MOD_PIKK_1 | 384 | 390 | PF00454 | 0.557 |
MOD_PIKK_1 | 400 | 406 | PF00454 | 0.773 |
MOD_PK_1 | 119 | 125 | PF00069 | 0.556 |
MOD_PKA_1 | 384 | 390 | PF00069 | 0.531 |
MOD_PKA_2 | 295 | 301 | PF00069 | 0.605 |
MOD_PKA_2 | 332 | 338 | PF00069 | 0.618 |
MOD_PKA_2 | 406 | 412 | PF00069 | 0.652 |
MOD_PKA_2 | 416 | 422 | PF00069 | 0.580 |
MOD_Plk_1 | 119 | 125 | PF00069 | 0.352 |
MOD_Plk_1 | 3 | 9 | PF00069 | 0.456 |
MOD_Plk_1 | 84 | 90 | PF00069 | 0.385 |
MOD_Plk_2-3 | 85 | 91 | PF00069 | 0.511 |
MOD_Plk_4 | 131 | 137 | PF00069 | 0.415 |
MOD_Plk_4 | 16 | 22 | PF00069 | 0.445 |
MOD_Plk_4 | 192 | 198 | PF00069 | 0.467 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.439 |
MOD_Plk_4 | 85 | 91 | PF00069 | 0.450 |
MOD_Plk_4 | 96 | 102 | PF00069 | 0.334 |
MOD_ProDKin_1 | 156 | 162 | PF00069 | 0.548 |
MOD_ProDKin_1 | 309 | 315 | PF00069 | 0.507 |
MOD_SUMO_rev_2 | 177 | 185 | PF00179 | 0.538 |
TRG_DiLeu_BaLyEn_6 | 20 | 25 | PF01217 | 0.267 |
TRG_ENDOCYTIC_2 | 137 | 140 | PF00928 | 0.475 |
TRG_ENDOCYTIC_2 | 150 | 153 | PF00928 | 0.313 |
TRG_ENDOCYTIC_2 | 213 | 216 | PF00928 | 0.620 |
TRG_ER_diArg_1 | 255 | 258 | PF00400 | 0.690 |
TRG_ER_diArg_1 | 316 | 318 | PF00400 | 0.732 |
TRG_ER_diArg_1 | 374 | 377 | PF00400 | 0.518 |
TRG_ER_diArg_1 | 429 | 431 | PF00400 | 0.507 |
TRG_NLS_Bipartite_1 | 183 | 203 | PF00514 | 0.580 |
TRG_NLS_MonoCore_2 | 314 | 319 | PF00514 | 0.668 |
TRG_NLS_MonoCore_2 | 382 | 387 | PF00514 | 0.541 |
TRG_NLS_MonoExtC_3 | 314 | 320 | PF00514 | 0.608 |
TRG_NLS_MonoExtN_4 | 198 | 203 | PF00514 | 0.567 |
TRG_NLS_MonoExtN_4 | 313 | 319 | PF00514 | 0.644 |
TRG_NLS_MonoExtN_4 | 380 | 387 | PF00514 | 0.557 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PC45 | Leptomonas seymouri | 58% | 100% |
A0A0S4KRJ3 | Bodo saltans | 30% | 100% |
A0A1X0NWC9 | Trypanosomatidae | 32% | 100% |
A0A3S7WVY2 | Leishmania donovani | 76% | 100% |
A0A422NPI7 | Trypanosoma rangeli | 37% | 100% |
A4HYT6 | Leishmania infantum | 76% | 94% |
C9ZIB2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
E9AUN2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 72% | 99% |
Q4QCV2 | Leishmania major | 77% | 100% |
V5DRZ7 | Trypanosoma cruzi | 37% | 100% |