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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005576 | extracellular region | 2 | 6 |
GO:0016020 | membrane | 2 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
Related structures:
AlphaFold database: Q4Q0V0
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0016787 | hydrolase activity | 2 | 7 |
GO:0008233 | peptidase activity | 3 | 1 |
GO:0008236 | serine-type peptidase activity | 4 | 1 |
GO:0017171 | serine hydrolase activity | 3 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 1 |
GO:0030600 | feruloyl esterase activity | 5 | 1 |
GO:0052689 | carboxylic ester hydrolase activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 24 | 28 | PF00656 | 0.689 |
CLV_C14_Caspase3-7 | 78 | 82 | PF00656 | 0.389 |
CLV_C14_Caspase3-7 | 91 | 95 | PF00656 | 0.277 |
CLV_NRD_NRD_1 | 30 | 32 | PF00675 | 0.472 |
CLV_NRD_NRD_1 | 359 | 361 | PF00675 | 0.593 |
CLV_NRD_NRD_1 | 429 | 431 | PF00675 | 0.707 |
CLV_NRD_NRD_1 | 470 | 472 | PF00675 | 0.661 |
CLV_NRD_NRD_1 | 510 | 512 | PF00675 | 0.717 |
CLV_PCSK_KEX2_1 | 168 | 170 | PF00082 | 0.438 |
CLV_PCSK_KEX2_1 | 429 | 431 | PF00082 | 0.708 |
CLV_PCSK_KEX2_1 | 448 | 450 | PF00082 | 0.583 |
CLV_PCSK_KEX2_1 | 510 | 512 | PF00082 | 0.697 |
CLV_PCSK_PC1ET2_1 | 168 | 170 | PF00082 | 0.431 |
CLV_PCSK_PC1ET2_1 | 448 | 450 | PF00082 | 0.659 |
CLV_PCSK_PC7_1 | 425 | 431 | PF00082 | 0.680 |
CLV_PCSK_SKI1_1 | 168 | 172 | PF00082 | 0.604 |
CLV_PCSK_SKI1_1 | 31 | 35 | PF00082 | 0.452 |
CLV_PCSK_SKI1_1 | 42 | 46 | PF00082 | 0.242 |
CLV_PCSK_SKI1_1 | 430 | 434 | PF00082 | 0.713 |
CLV_PCSK_SKI1_1 | 455 | 459 | PF00082 | 0.636 |
CLV_Separin_Metazoa | 545 | 549 | PF03568 | 0.390 |
DEG_SCF_SKP2-CKS1_1 | 15 | 22 | PF00560 | 0.636 |
DOC_CYCLIN_yCln2_LP_2 | 52 | 58 | PF00134 | 0.386 |
DOC_MAPK_gen_1 | 121 | 129 | PF00069 | 0.322 |
DOC_MAPK_gen_1 | 510 | 517 | PF00069 | 0.518 |
DOC_MAPK_gen_1 | 522 | 529 | PF00069 | 0.431 |
DOC_MAPK_gen_1 | 66 | 75 | PF00069 | 0.394 |
DOC_MAPK_JIP1_4 | 152 | 158 | PF00069 | 0.296 |
DOC_MAPK_JIP1_4 | 511 | 517 | PF00069 | 0.452 |
DOC_MAPK_MEF2A_6 | 152 | 160 | PF00069 | 0.323 |
DOC_PP1_RVXF_1 | 314 | 321 | PF00149 | 0.327 |
DOC_PP1_RVXF_1 | 556 | 563 | PF00149 | 0.347 |
DOC_PP2B_LxvP_1 | 26 | 29 | PF13499 | 0.698 |
DOC_PP2B_LxvP_1 | 308 | 311 | PF13499 | 0.338 |
DOC_PP2B_LxvP_1 | 52 | 55 | PF13499 | 0.386 |
DOC_USP7_MATH_1 | 263 | 267 | PF00917 | 0.261 |
DOC_USP7_MATH_1 | 295 | 299 | PF00917 | 0.279 |
DOC_USP7_MATH_1 | 516 | 520 | PF00917 | 0.478 |
DOC_USP7_UBL2_3 | 18 | 22 | PF12436 | 0.642 |
DOC_USP7_UBL2_3 | 458 | 462 | PF12436 | 0.514 |
DOC_WW_Pin1_4 | 16 | 21 | PF00397 | 0.683 |
LIG_14-3-3_CanoR_1 | 262 | 268 | PF00244 | 0.328 |
LIG_14-3-3_CanoR_1 | 296 | 300 | PF00244 | 0.317 |
LIG_14-3-3_CanoR_1 | 42 | 47 | PF00244 | 0.324 |
LIG_14-3-3_CanoR_1 | 434 | 440 | PF00244 | 0.434 |
LIG_APCC_ABBA_1 | 176 | 181 | PF00400 | 0.253 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.646 |
LIG_BIR_III_2 | 27 | 31 | PF00653 | 0.679 |
LIG_BIR_III_4 | 10 | 14 | PF00653 | 0.635 |
LIG_BRCT_BRCA1_1 | 480 | 484 | PF00533 | 0.493 |
LIG_BRCT_BRCA1_1 | 79 | 83 | PF00533 | 0.428 |
LIG_EH1_1 | 82 | 90 | PF00400 | 0.397 |
LIG_FHA_1 | 172 | 178 | PF00498 | 0.253 |
LIG_FHA_1 | 283 | 289 | PF00498 | 0.334 |
LIG_FHA_1 | 295 | 301 | PF00498 | 0.317 |
LIG_FHA_1 | 303 | 309 | PF00498 | 0.234 |
LIG_FHA_1 | 539 | 545 | PF00498 | 0.339 |
LIG_FHA_1 | 563 | 569 | PF00498 | 0.286 |
LIG_FHA_2 | 133 | 139 | PF00498 | 0.349 |
LIG_FHA_2 | 376 | 382 | PF00498 | 0.503 |
LIG_FHA_2 | 399 | 405 | PF00498 | 0.438 |
LIG_IBAR_NPY_1 | 383 | 385 | PF08397 | 0.434 |
LIG_LIR_Gen_1 | 183 | 190 | PF02991 | 0.296 |
LIG_LIR_Gen_1 | 418 | 427 | PF02991 | 0.456 |
LIG_LIR_Gen_1 | 60 | 68 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 128 | 132 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 174 | 179 | PF02991 | 0.275 |
LIG_LIR_Nem_3 | 183 | 188 | PF02991 | 0.275 |
LIG_LIR_Nem_3 | 259 | 264 | PF02991 | 0.312 |
LIG_LIR_Nem_3 | 418 | 424 | PF02991 | 0.453 |
LIG_PCNA_yPIPBox_3 | 82 | 90 | PF02747 | 0.365 |
LIG_PTAP_UEV_1 | 147 | 152 | PF05743 | 0.231 |
LIG_PTB_Apo_2 | 348 | 355 | PF02174 | 0.329 |
LIG_PTB_Phospho_1 | 348 | 354 | PF10480 | 0.382 |
LIG_SH2_GRB2like | 349 | 352 | PF00017 | 0.329 |
LIG_SH2_GRB2like | 354 | 357 | PF00017 | 0.336 |
LIG_SH2_STAT5 | 100 | 103 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 142 | 145 | PF00017 | 0.275 |
LIG_SH2_STAT5 | 196 | 199 | PF00017 | 0.261 |
LIG_SH2_STAT5 | 349 | 352 | PF00017 | 0.329 |
LIG_SH2_STAT5 | 354 | 357 | PF00017 | 0.336 |
LIG_SH2_STAT5 | 421 | 424 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 491 | 494 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 567 | 570 | PF00017 | 0.293 |
LIG_SH2_STAT5 | 57 | 60 | PF00017 | 0.470 |
LIG_SH3_1 | 114 | 120 | PF00018 | 0.385 |
LIG_SH3_3 | 114 | 120 | PF00018 | 0.367 |
LIG_SH3_3 | 138 | 144 | PF00018 | 0.261 |
LIG_SH3_3 | 145 | 151 | PF00018 | 0.261 |
LIG_SH3_3 | 356 | 362 | PF00018 | 0.342 |
LIG_SUMO_SIM_anti_2 | 541 | 548 | PF11976 | 0.392 |
LIG_SUMO_SIM_anti_2 | 70 | 78 | PF11976 | 0.442 |
LIG_SUMO_SIM_par_1 | 70 | 78 | PF11976 | 0.449 |
LIG_TRFH_1 | 484 | 488 | PF08558 | 0.503 |
LIG_TYR_ITIM | 177 | 182 | PF00017 | 0.280 |
LIG_UBA3_1 | 159 | 168 | PF00899 | 0.328 |
LIG_WRC_WIRS_1 | 126 | 131 | PF05994 | 0.374 |
LIG_WRC_WIRS_1 | 366 | 371 | PF05994 | 0.436 |
LIG_WW_3 | 28 | 32 | PF00397 | 0.694 |
MOD_CDK_SPxK_1 | 16 | 22 | PF00069 | 0.637 |
MOD_CK1_1 | 103 | 109 | PF00069 | 0.387 |
MOD_CK1_1 | 146 | 152 | PF00069 | 0.275 |
MOD_CK1_1 | 16 | 22 | PF00069 | 0.716 |
MOD_CK1_1 | 345 | 351 | PF00069 | 0.389 |
MOD_CK1_1 | 74 | 80 | PF00069 | 0.430 |
MOD_CK2_1 | 132 | 138 | PF00069 | 0.301 |
MOD_CK2_1 | 33 | 39 | PF00069 | 0.583 |
MOD_CK2_1 | 375 | 381 | PF00069 | 0.483 |
MOD_CK2_1 | 397 | 403 | PF00069 | 0.539 |
MOD_CK2_1 | 412 | 418 | PF00069 | 0.410 |
MOD_CK2_1 | 539 | 545 | PF00069 | 0.372 |
MOD_GlcNHglycan | 267 | 270 | PF01048 | 0.496 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.320 |
MOD_GSK3_1 | 142 | 149 | PF00069 | 0.281 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.259 |
MOD_GSK3_1 | 290 | 297 | PF00069 | 0.417 |
MOD_GSK3_1 | 334 | 341 | PF00069 | 0.405 |
MOD_GSK3_1 | 345 | 352 | PF00069 | 0.345 |
MOD_GSK3_1 | 398 | 405 | PF00069 | 0.440 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.400 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.727 |
MOD_GSK3_1 | 99 | 106 | PF00069 | 0.387 |
MOD_LATS_1 | 470 | 476 | PF00433 | 0.458 |
MOD_N-GLC_1 | 355 | 360 | PF02516 | 0.597 |
MOD_N-GLC_1 | 392 | 397 | PF02516 | 0.703 |
MOD_N-GLC_1 | 538 | 543 | PF02516 | 0.554 |
MOD_N-GLC_2 | 334 | 336 | PF02516 | 0.548 |
MOD_NEK2_1 | 171 | 176 | PF00069 | 0.275 |
MOD_NEK2_1 | 227 | 232 | PF00069 | 0.328 |
MOD_NEK2_2 | 349 | 354 | PF00069 | 0.298 |
MOD_PIKK_1 | 225 | 231 | PF00454 | 0.253 |
MOD_PIKK_1 | 494 | 500 | PF00454 | 0.511 |
MOD_PIKK_1 | 539 | 545 | PF00454 | 0.365 |
MOD_PKA_1 | 31 | 37 | PF00069 | 0.643 |
MOD_PKA_1 | 471 | 477 | PF00069 | 0.449 |
MOD_PKA_2 | 295 | 301 | PF00069 | 0.381 |
MOD_PKA_2 | 433 | 439 | PF00069 | 0.483 |
MOD_Plk_1 | 233 | 239 | PF00069 | 0.290 |
MOD_Plk_1 | 355 | 361 | PF00069 | 0.406 |
MOD_Plk_1 | 402 | 408 | PF00069 | 0.420 |
MOD_Plk_4 | 100 | 106 | PF00069 | 0.357 |
MOD_Plk_4 | 122 | 128 | PF00069 | 0.373 |
MOD_Plk_4 | 295 | 301 | PF00069 | 0.317 |
MOD_Plk_4 | 319 | 325 | PF00069 | 0.409 |
MOD_Plk_4 | 345 | 351 | PF00069 | 0.369 |
MOD_ProDKin_1 | 16 | 22 | PF00069 | 0.686 |
MOD_SUMO_rev_2 | 461 | 468 | PF00179 | 0.512 |
TRG_DiLeu_BaEn_2 | 180 | 186 | PF01217 | 0.261 |
TRG_ENDOCYTIC_2 | 179 | 182 | PF00928 | 0.280 |
TRG_ENDOCYTIC_2 | 385 | 388 | PF00928 | 0.491 |
TRG_ENDOCYTIC_2 | 421 | 424 | PF00928 | 0.450 |
TRG_ER_diArg_1 | 510 | 512 | PF00400 | 0.500 |
TRG_NES_CRM1_1 | 222 | 234 | PF08389 | 0.223 |
TRG_Pf-PMV_PEXEL_1 | 90 | 94 | PF00026 | 0.501 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PD17 | Leptomonas seymouri | 43% | 100% |
A0A3S7XBJ7 | Leishmania donovani | 84% | 99% |
A4HPY1 | Leishmania braziliensis | 57% | 99% |
A4IDP2 | Leishmania infantum | 84% | 99% |
E9ATP8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 99% |