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: A0A3S7WVY2
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_NRD_NRD_1 | 257 | 259 | PF00675 | 0.697 |
CLV_NRD_NRD_1 | 316 | 318 | PF00675 | 0.630 |
CLV_NRD_NRD_1 | 377 | 379 | PF00675 | 0.495 |
CLV_NRD_NRD_1 | 387 | 389 | PF00675 | 0.568 |
CLV_PCSK_FUR_1 | 254 | 258 | PF00082 | 0.734 |
CLV_PCSK_FUR_1 | 427 | 431 | PF00082 | 0.496 |
CLV_PCSK_KEX2_1 | 183 | 185 | PF00082 | 0.526 |
CLV_PCSK_KEX2_1 | 256 | 258 | PF00082 | 0.679 |
CLV_PCSK_KEX2_1 | 314 | 316 | PF00082 | 0.551 |
CLV_PCSK_KEX2_1 | 387 | 389 | PF00082 | 0.569 |
CLV_PCSK_KEX2_1 | 429 | 431 | PF00082 | 0.596 |
CLV_PCSK_PC1ET2_1 | 183 | 185 | PF00082 | 0.433 |
CLV_PCSK_PC1ET2_1 | 314 | 316 | PF00082 | 0.551 |
CLV_PCSK_PC1ET2_1 | 429 | 431 | PF00082 | 0.780 |
CLV_PCSK_SKI1_1 | 382 | 386 | PF00082 | 0.560 |
CLV_PCSK_SKI1_1 | 98 | 102 | PF00082 | 0.363 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.322 |
DEG_SPOP_SBC_1 | 391 | 395 | PF00917 | 0.577 |
DOC_CKS1_1 | 157 | 162 | PF01111 | 0.444 |
DOC_CKS1_1 | 62 | 67 | PF01111 | 0.476 |
DOC_CYCLIN_yCln2_LP_2 | 43 | 49 | PF00134 | 0.382 |
DOC_MAPK_FxFP_2 | 7 | 10 | PF00069 | 0.307 |
DOC_MAPK_gen_1 | 28 | 37 | PF00069 | 0.371 |
DOC_MAPK_gen_1 | 83 | 92 | PF00069 | 0.340 |
DOC_PP2B_LxvP_1 | 140 | 143 | PF13499 | 0.540 |
DOC_PP2B_LxvP_1 | 43 | 46 | PF13499 | 0.486 |
DOC_PP4_FxxP_1 | 20 | 23 | PF00568 | 0.458 |
DOC_PP4_FxxP_1 | 7 | 10 | PF00568 | 0.343 |
DOC_USP7_MATH_1 | 125 | 129 | PF00917 | 0.556 |
DOC_USP7_MATH_1 | 222 | 226 | PF00917 | 0.659 |
DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.494 |
DOC_USP7_MATH_1 | 244 | 248 | PF00917 | 0.528 |
DOC_USP7_MATH_1 | 287 | 291 | PF00917 | 0.746 |
DOC_USP7_MATH_1 | 309 | 313 | PF00917 | 0.644 |
DOC_USP7_MATH_1 | 389 | 393 | PF00917 | 0.672 |
DOC_USP7_MATH_1 | 412 | 416 | PF00917 | 0.662 |
DOC_USP7_MATH_2 | 46 | 52 | PF00917 | 0.349 |
DOC_USP7_UBL2_3 | 420 | 424 | PF12436 | 0.737 |
DOC_USP7_UBL2_3 | 425 | 429 | PF12436 | 0.647 |
DOC_WW_Pin1_4 | 156 | 161 | PF00397 | 0.556 |
DOC_WW_Pin1_4 | 266 | 271 | PF00397 | 0.525 |
DOC_WW_Pin1_4 | 334 | 339 | PF00397 | 0.459 |
DOC_WW_Pin1_4 | 61 | 66 | PF00397 | 0.511 |
LIG_14-3-3_CanoR_1 | 109 | 113 | PF00244 | 0.546 |
LIG_14-3-3_CanoR_1 | 119 | 124 | PF00244 | 0.445 |
LIG_14-3-3_CanoR_1 | 184 | 193 | PF00244 | 0.458 |
LIG_14-3-3_CanoR_1 | 28 | 37 | PF00244 | 0.330 |
LIG_14-3-3_CanoR_1 | 332 | 338 | PF00244 | 0.643 |
LIG_14-3-3_CanoR_1 | 54 | 62 | PF00244 | 0.426 |
LIG_Actin_WH2_2 | 168 | 185 | PF00022 | 0.504 |
LIG_BRCT_BRCA1_1 | 289 | 293 | PF00533 | 0.613 |
LIG_BRCT_BRCA1_1 | 296 | 300 | PF00533 | 0.585 |
LIG_BRCT_BRCA1_1 | 414 | 418 | PF00533 | 0.546 |
LIG_BRCT_BRCA1_1 | 5 | 9 | PF00533 | 0.444 |
LIG_BRCT_BRCA1_2 | 289 | 295 | PF00533 | 0.645 |
LIG_BRCT_BRCA1_2 | 296 | 302 | PF00533 | 0.612 |
LIG_BRCT_BRCA1_2 | 414 | 420 | PF00533 | 0.543 |
LIG_FHA_1 | 174 | 180 | PF00498 | 0.413 |
LIG_FHA_1 | 331 | 337 | PF00498 | 0.561 |
LIG_FHA_1 | 95 | 101 | PF00498 | 0.386 |
LIG_FHA_2 | 156 | 162 | PF00498 | 0.531 |
LIG_FHA_2 | 54 | 60 | PF00498 | 0.468 |
LIG_LIR_Apic_2 | 19 | 23 | PF02991 | 0.457 |
LIG_LIR_Apic_2 | 4 | 10 | PF02991 | 0.321 |
LIG_LIR_Apic_2 | 59 | 65 | PF02991 | 0.471 |
LIG_LIR_Gen_1 | 148 | 157 | PF02991 | 0.355 |
LIG_LIR_Gen_1 | 212 | 221 | PF02991 | 0.395 |
LIG_LIR_Gen_1 | 349 | 356 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 134 | 140 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 148 | 154 | PF02991 | 0.343 |
LIG_LIR_Nem_3 | 165 | 169 | PF02991 | 0.549 |
LIG_LIR_Nem_3 | 19 | 24 | PF02991 | 0.489 |
LIG_LIR_Nem_3 | 212 | 216 | PF02991 | 0.618 |
LIG_LIR_Nem_3 | 290 | 296 | PF02991 | 0.626 |
LIG_LIR_Nem_3 | 349 | 354 | PF02991 | 0.569 |
LIG_LIR_Nem_3 | 99 | 104 | PF02991 | 0.329 |
LIG_MLH1_MIPbox_1 | 290 | 294 | PF16413 | 0.603 |
LIG_REV1ctd_RIR_1 | 291 | 299 | PF16727 | 0.549 |
LIG_REV1ctd_RIR_1 | 351 | 359 | PF16727 | 0.610 |
LIG_SH2_CRK | 137 | 141 | PF00017 | 0.499 |
LIG_SH2_NCK_1 | 62 | 66 | PF00017 | 0.482 |
LIG_SH2_PTP2 | 151 | 154 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 151 | 154 | PF00017 | 0.378 |
LIG_SH2_STAT5 | 213 | 216 | PF00017 | 0.537 |
LIG_SH3_3 | 154 | 160 | PF00018 | 0.472 |
LIG_SUMO_SIM_par_1 | 88 | 97 | PF11976 | 0.337 |
LIG_TYR_ITIM | 135 | 140 | PF00017 | 0.476 |
LIG_TYR_ITIM | 211 | 216 | PF00017 | 0.589 |
LIG_WRC_WIRS_1 | 216 | 221 | PF05994 | 0.393 |
MOD_CK1_1 | 113 | 119 | PF00069 | 0.412 |
MOD_CK1_1 | 217 | 223 | PF00069 | 0.686 |
MOD_CK1_1 | 269 | 275 | PF00069 | 0.647 |
MOD_CK1_1 | 392 | 398 | PF00069 | 0.673 |
MOD_CK1_1 | 407 | 413 | PF00069 | 0.512 |
MOD_CK1_1 | 94 | 100 | PF00069 | 0.390 |
MOD_CK2_1 | 155 | 161 | PF00069 | 0.478 |
MOD_CK2_1 | 334 | 340 | PF00069 | 0.588 |
MOD_CK2_1 | 53 | 59 | PF00069 | 0.448 |
MOD_CK2_1 | 85 | 91 | PF00069 | 0.463 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.561 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.385 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.690 |
MOD_GlcNHglycan | 271 | 274 | PF01048 | 0.704 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.614 |
MOD_GlcNHglycan | 296 | 299 | PF01048 | 0.609 |
MOD_GlcNHglycan | 306 | 309 | PF01048 | 0.654 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.463 |
MOD_GlcNHglycan | 395 | 398 | PF01048 | 0.655 |
MOD_GlcNHglycan | 407 | 410 | PF01048 | 0.688 |
MOD_GlcNHglycan | 414 | 417 | PF01048 | 0.738 |
MOD_GlcNHglycan | 50 | 53 | PF01048 | 0.343 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.345 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.502 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.582 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.579 |
MOD_GSK3_1 | 389 | 396 | PF00069 | 0.710 |
MOD_GSK3_1 | 399 | 406 | PF00069 | 0.586 |
MOD_GSK3_1 | 412 | 419 | PF00069 | 0.668 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.364 |
MOD_NEK2_1 | 123 | 128 | PF00069 | 0.362 |
MOD_NEK2_1 | 174 | 179 | PF00069 | 0.393 |
MOD_NEK2_1 | 211 | 216 | PF00069 | 0.515 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.560 |
MOD_NEK2_1 | 294 | 299 | PF00069 | 0.493 |
MOD_NEK2_1 | 331 | 336 | PF00069 | 0.542 |
MOD_NEK2_1 | 37 | 42 | PF00069 | 0.355 |
MOD_NEK2_1 | 418 | 423 | PF00069 | 0.741 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.342 |
MOD_NEK2_2 | 327 | 332 | PF00069 | 0.430 |
MOD_PIKK_1 | 142 | 148 | PF00454 | 0.475 |
MOD_PIKK_1 | 184 | 190 | PF00454 | 0.565 |
MOD_PIKK_1 | 23 | 29 | PF00454 | 0.328 |
MOD_PIKK_1 | 399 | 405 | PF00454 | 0.768 |
MOD_PKA_2 | 108 | 114 | PF00069 | 0.536 |
MOD_PKA_2 | 242 | 248 | PF00069 | 0.754 |
MOD_PKA_2 | 331 | 337 | PF00069 | 0.537 |
MOD_PKA_2 | 53 | 59 | PF00069 | 0.417 |
MOD_Plk_1 | 211 | 217 | PF00069 | 0.426 |
MOD_Plk_1 | 3 | 9 | PF00069 | 0.430 |
MOD_Plk_2-3 | 85 | 91 | PF00069 | 0.469 |
MOD_Plk_4 | 131 | 137 | PF00069 | 0.355 |
MOD_Plk_4 | 16 | 22 | PF00069 | 0.483 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.461 |
MOD_Plk_4 | 85 | 91 | PF00069 | 0.389 |
MOD_Plk_4 | 96 | 102 | PF00069 | 0.308 |
MOD_ProDKin_1 | 156 | 162 | PF00069 | 0.556 |
MOD_ProDKin_1 | 266 | 272 | PF00069 | 0.526 |
MOD_ProDKin_1 | 334 | 340 | PF00069 | 0.458 |
MOD_ProDKin_1 | 61 | 67 | PF00069 | 0.510 |
MOD_SUMO_rev_2 | 177 | 185 | PF00179 | 0.396 |
TRG_ENDOCYTIC_2 | 137 | 140 | PF00928 | 0.473 |
TRG_ENDOCYTIC_2 | 150 | 153 | PF00928 | 0.312 |
TRG_ENDOCYTIC_2 | 213 | 216 | PF00928 | 0.600 |
TRG_ER_diArg_1 | 206 | 209 | PF00400 | 0.432 |
TRG_ER_diArg_1 | 254 | 257 | PF00400 | 0.656 |
TRG_ER_diArg_1 | 315 | 317 | PF00400 | 0.704 |
TRG_NLS_Bipartite_1 | 183 | 203 | PF00514 | 0.440 |
TRG_NLS_MonoCore_2 | 313 | 318 | PF00514 | 0.605 |
TRG_NLS_MonoExtC_3 | 313 | 319 | PF00514 | 0.543 |
TRG_NLS_MonoExtC_3 | 423 | 428 | PF00514 | 0.743 |
TRG_NLS_MonoExtN_4 | 198 | 203 | PF00514 | 0.427 |
TRG_NLS_MonoExtN_4 | 311 | 318 | PF00514 | 0.579 |
TRG_NLS_MonoExtN_4 | 423 | 428 | PF00514 | 0.689 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PC45 | Leptomonas seymouri | 57% | 100% |
A0A0S4KRJ3 | Bodo saltans | 32% | 100% |
A0A1X0NWC9 | Trypanosomatidae | 34% | 100% |
A0A422NPI7 | Trypanosoma rangeli | 35% | 100% |
A4HYT6 | Leishmania infantum | 99% | 100% |
C9ZIB2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
E9AIE5 | Leishmania braziliensis | 76% | 100% |
E9AUN2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
Q4QCV2 | Leishmania major | 90% | 100% |
V5DRZ7 | Trypanosoma cruzi | 38% | 100% |