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: 1, no: 26 |
NetGPI | no | yes: 0, no: 27 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AUQ8
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 28 |
GO:0006807 | nitrogen compound metabolic process | 2 | 28 |
GO:0008152 | metabolic process | 1 | 28 |
GO:0019538 | protein metabolic process | 3 | 28 |
GO:0043170 | macromolecule metabolic process | 3 | 28 |
GO:0044238 | primary metabolic process | 2 | 28 |
GO:0071704 | organic substance metabolic process | 2 | 28 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 28 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 28 |
GO:0004175 | endopeptidase activity | 4 | 28 |
GO:0004197 | cysteine-type endopeptidase activity | 5 | 28 |
GO:0004198 | calcium-dependent cysteine-type endopeptidase activity | 6 | 28 |
GO:0008233 | peptidase activity | 3 | 28 |
GO:0008234 | cysteine-type peptidase activity | 4 | 28 |
GO:0016787 | hydrolase activity | 2 | 28 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 28 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 447 | 451 | PF00656 | 0.569 |
CLV_NRD_NRD_1 | 451 | 453 | PF00675 | 0.208 |
CLV_PCSK_KEX2_1 | 504 | 506 | PF00082 | 0.453 |
CLV_PCSK_KEX2_1 | 604 | 606 | PF00082 | 0.312 |
CLV_PCSK_KEX2_1 | 634 | 636 | PF00082 | 0.532 |
CLV_PCSK_PC1ET2_1 | 504 | 506 | PF00082 | 0.432 |
CLV_PCSK_PC1ET2_1 | 604 | 606 | PF00082 | 0.295 |
CLV_PCSK_PC1ET2_1 | 634 | 636 | PF00082 | 0.574 |
CLV_PCSK_SKI1_1 | 133 | 137 | PF00082 | 0.548 |
CLV_PCSK_SKI1_1 | 277 | 281 | PF00082 | 0.205 |
CLV_PCSK_SKI1_1 | 399 | 403 | PF00082 | 0.315 |
DEG_Kelch_Keap1_1 | 4 | 9 | PF01344 | 0.544 |
DEG_SIAH_1 | 123 | 131 | PF03145 | 0.472 |
DOC_PP4_FxxP_1 | 195 | 198 | PF00568 | 0.388 |
DOC_USP7_UBL2_3 | 295 | 299 | PF12436 | 0.509 |
DOC_USP7_UBL2_3 | 449 | 453 | PF12436 | 0.437 |
DOC_WW_Pin1_4 | 355 | 360 | PF00397 | 0.528 |
DOC_WW_Pin1_4 | 488 | 493 | PF00397 | 0.329 |
LIG_14-3-3_CanoR_1 | 133 | 139 | PF00244 | 0.424 |
LIG_14-3-3_CanoR_1 | 541 | 550 | PF00244 | 0.421 |
LIG_Actin_WH2_2 | 262 | 279 | PF00022 | 0.395 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.536 |
LIG_BIR_III_2 | 425 | 429 | PF00653 | 0.395 |
LIG_BRCT_BRCA1_1 | 599 | 603 | PF00533 | 0.497 |
LIG_Clathr_ClatBox_1 | 623 | 627 | PF01394 | 0.308 |
LIG_deltaCOP1_diTrp_1 | 412 | 417 | PF00928 | 0.471 |
LIG_deltaCOP1_diTrp_1 | 545 | 549 | PF00928 | 0.394 |
LIG_eIF4E_1 | 374 | 380 | PF01652 | 0.625 |
LIG_FHA_1 | 130 | 136 | PF00498 | 0.446 |
LIG_FHA_1 | 475 | 481 | PF00498 | 0.522 |
LIG_FHA_1 | 494 | 500 | PF00498 | 0.408 |
LIG_FHA_2 | 384 | 390 | PF00498 | 0.441 |
LIG_FHA_2 | 420 | 426 | PF00498 | 0.508 |
LIG_LIR_Apic_2 | 193 | 198 | PF02991 | 0.198 |
LIG_LIR_Apic_2 | 91 | 97 | PF02991 | 0.535 |
LIG_LIR_Gen_1 | 294 | 304 | PF02991 | 0.524 |
LIG_LIR_Gen_1 | 320 | 327 | PF02991 | 0.485 |
LIG_LIR_Gen_1 | 338 | 349 | PF02991 | 0.491 |
LIG_LIR_Gen_1 | 372 | 380 | PF02991 | 0.531 |
LIG_LIR_Gen_1 | 493 | 499 | PF02991 | 0.337 |
LIG_LIR_Gen_1 | 544 | 555 | PF02991 | 0.455 |
LIG_LIR_Gen_1 | 57 | 66 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 209 | 215 | PF02991 | 0.197 |
LIG_LIR_Nem_3 | 248 | 254 | PF02991 | 0.518 |
LIG_LIR_Nem_3 | 266 | 271 | PF02991 | 0.542 |
LIG_LIR_Nem_3 | 287 | 292 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 294 | 300 | PF02991 | 0.511 |
LIG_LIR_Nem_3 | 303 | 307 | PF02991 | 0.514 |
LIG_LIR_Nem_3 | 338 | 344 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 372 | 377 | PF02991 | 0.534 |
LIG_LIR_Nem_3 | 493 | 498 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 511 | 516 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 527 | 532 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 544 | 550 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 57 | 61 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 600 | 606 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 614 | 619 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 7 | 13 | PF02991 | 0.690 |
LIG_Pex14_2 | 444 | 448 | PF04695 | 0.542 |
LIG_Pex14_2 | 54 | 58 | PF04695 | 0.488 |
LIG_SH2_CRK | 297 | 301 | PF00017 | 0.509 |
LIG_SH2_CRK | 304 | 308 | PF00017 | 0.504 |
LIG_SH2_CRK | 352 | 356 | PF00017 | 0.477 |
LIG_SH2_CRK | 374 | 378 | PF00017 | 0.509 |
LIG_SH2_CRK | 513 | 517 | PF00017 | 0.474 |
LIG_SH2_CRK | 529 | 533 | PF00017 | 0.477 |
LIG_SH2_CRK | 94 | 98 | PF00017 | 0.772 |
LIG_SH2_GRB2like | 454 | 457 | PF00017 | 0.437 |
LIG_SH2_NCK_1 | 374 | 378 | PF00017 | 0.493 |
LIG_SH2_NCK_1 | 94 | 98 | PF00017 | 0.552 |
LIG_SH2_PTP2 | 566 | 569 | PF00017 | 0.390 |
LIG_SH2_SRC | 268 | 271 | PF00017 | 0.539 |
LIG_SH2_SRC | 392 | 395 | PF00017 | 0.538 |
LIG_SH2_STAP1 | 221 | 225 | PF00017 | 0.210 |
LIG_SH2_STAP1 | 278 | 282 | PF00017 | 0.562 |
LIG_SH2_STAP1 | 468 | 472 | PF00017 | 0.357 |
LIG_SH2_STAP1 | 64 | 68 | PF00017 | 0.401 |
LIG_SH2_STAT3 | 32 | 35 | PF00017 | 0.721 |
LIG_SH2_STAT5 | 251 | 254 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 268 | 271 | PF00017 | 0.524 |
LIG_SH2_STAT5 | 352 | 355 | PF00017 | 0.554 |
LIG_SH2_STAT5 | 385 | 388 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 392 | 395 | PF00017 | 0.467 |
LIG_SH2_STAT5 | 454 | 457 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 566 | 569 | PF00017 | 0.374 |
LIG_SH2_STAT5 | 584 | 587 | PF00017 | 0.410 |
LIG_SH3_3 | 100 | 106 | PF00018 | 0.529 |
LIG_SH3_3 | 486 | 492 | PF00018 | 0.376 |
LIG_SH3_3 | 575 | 581 | PF00018 | 0.514 |
LIG_SH3_3 | 623 | 629 | PF00018 | 0.474 |
LIG_SUMO_SIM_anti_2 | 554 | 560 | PF11976 | 0.232 |
LIG_SUMO_SIM_par_1 | 482 | 488 | PF11976 | 0.411 |
LIG_SUMO_SIM_par_1 | 514 | 519 | PF11976 | 0.427 |
LIG_TRAF2_1 | 33 | 36 | PF00917 | 0.680 |
LIG_TRAF2_1 | 41 | 44 | PF00917 | 0.536 |
LIG_TRAF2_1 | 77 | 80 | PF00917 | 0.535 |
LIG_TRAF2_1 | 82 | 85 | PF00917 | 0.534 |
LIG_TYR_ITIM | 200 | 205 | PF00017 | 0.197 |
LIG_UBA3_1 | 200 | 208 | PF00899 | 0.197 |
LIG_UBA3_1 | 443 | 449 | PF00899 | 0.395 |
LIG_UBA3_1 | 557 | 565 | PF00899 | 0.251 |
LIG_WRC_WIRS_1 | 251 | 256 | PF05994 | 0.465 |
MOD_CDK_SPxK_1 | 355 | 361 | PF00069 | 0.553 |
MOD_CK2_1 | 149 | 155 | PF00069 | 0.463 |
MOD_CK2_1 | 30 | 36 | PF00069 | 0.562 |
MOD_CK2_1 | 383 | 389 | PF00069 | 0.473 |
MOD_CK2_1 | 516 | 522 | PF00069 | 0.389 |
MOD_CMANNOS | 445 | 448 | PF00535 | 0.293 |
MOD_GlcNHglycan | 107 | 110 | PF01048 | 0.677 |
MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.727 |
MOD_GlcNHglycan | 271 | 274 | PF01048 | 0.351 |
MOD_GlcNHglycan | 280 | 283 | PF01048 | 0.349 |
MOD_GlcNHglycan | 308 | 311 | PF01048 | 0.286 |
MOD_GlcNHglycan | 412 | 416 | PF01048 | 0.362 |
MOD_GlcNHglycan | 481 | 484 | PF01048 | 0.415 |
MOD_GlcNHglycan | 535 | 538 | PF01048 | 0.428 |
MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.612 |
MOD_GSK3_1 | 317 | 324 | PF00069 | 0.513 |
MOD_GSK3_1 | 350 | 357 | PF00069 | 0.528 |
MOD_GSK3_1 | 407 | 414 | PF00069 | 0.462 |
MOD_GSK3_1 | 493 | 500 | PF00069 | 0.396 |
MOD_GSK3_1 | 541 | 548 | PF00069 | 0.488 |
MOD_N-GLC_1 | 215 | 220 | PF02516 | 0.197 |
MOD_N-GLC_1 | 239 | 244 | PF02516 | 0.432 |
MOD_N-GLC_1 | 508 | 513 | PF02516 | 0.336 |
MOD_N-GLC_1 | 533 | 538 | PF02516 | 0.396 |
MOD_NEK2_1 | 156 | 161 | PF00069 | 0.449 |
MOD_NEK2_1 | 238 | 243 | PF00069 | 0.376 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.517 |
MOD_NEK2_1 | 327 | 332 | PF00069 | 0.525 |
MOD_NEK2_1 | 444 | 449 | PF00069 | 0.501 |
MOD_NEK2_1 | 533 | 538 | PF00069 | 0.362 |
MOD_NEK2_2 | 321 | 326 | PF00069 | 0.395 |
MOD_NEK2_2 | 597 | 602 | PF00069 | 0.281 |
MOD_PIKK_1 | 31 | 37 | PF00454 | 0.659 |
MOD_PIKK_1 | 497 | 503 | PF00454 | 0.449 |
MOD_PIKK_1 | 641 | 647 | PF00454 | 0.429 |
MOD_PKA_2 | 540 | 546 | PF00069 | 0.505 |
MOD_Plk_1 | 175 | 181 | PF00069 | 0.438 |
MOD_Plk_1 | 215 | 221 | PF00069 | 0.327 |
MOD_Plk_1 | 238 | 244 | PF00069 | 0.270 |
MOD_Plk_1 | 25 | 31 | PF00069 | 0.611 |
MOD_Plk_1 | 327 | 333 | PF00069 | 0.498 |
MOD_Plk_1 | 553 | 559 | PF00069 | 0.350 |
MOD_Plk_1 | 597 | 603 | PF00069 | 0.353 |
MOD_Plk_2-3 | 329 | 335 | PF00069 | 0.395 |
MOD_Plk_4 | 175 | 181 | PF00069 | 0.703 |
MOD_Plk_4 | 264 | 270 | PF00069 | 0.515 |
MOD_Plk_4 | 350 | 356 | PF00069 | 0.557 |
MOD_Plk_4 | 383 | 389 | PF00069 | 0.523 |
MOD_Plk_4 | 553 | 559 | PF00069 | 0.401 |
MOD_ProDKin_1 | 355 | 361 | PF00069 | 0.528 |
MOD_ProDKin_1 | 488 | 494 | PF00069 | 0.325 |
MOD_SUMO_for_1 | 187 | 190 | PF00179 | 0.197 |
MOD_SUMO_for_1 | 617 | 620 | PF00179 | 0.329 |
MOD_SUMO_rev_2 | 328 | 337 | PF00179 | 0.478 |
MOD_SUMO_rev_2 | 389 | 398 | PF00179 | 0.511 |
MOD_SUMO_rev_2 | 511 | 516 | PF00179 | 0.505 |
MOD_SUMO_rev_2 | 65 | 70 | PF00179 | 0.633 |
TRG_DiLeu_BaEn_4 | 15 | 21 | PF01217 | 0.547 |
TRG_ENDOCYTIC_2 | 202 | 205 | PF00928 | 0.197 |
TRG_ENDOCYTIC_2 | 251 | 254 | PF00928 | 0.537 |
TRG_ENDOCYTIC_2 | 268 | 271 | PF00928 | 0.540 |
TRG_ENDOCYTIC_2 | 297 | 300 | PF00928 | 0.510 |
TRG_ENDOCYTIC_2 | 304 | 307 | PF00928 | 0.506 |
TRG_ENDOCYTIC_2 | 352 | 355 | PF00928 | 0.479 |
TRG_ENDOCYTIC_2 | 374 | 377 | PF00928 | 0.525 |
TRG_ENDOCYTIC_2 | 385 | 388 | PF00928 | 0.533 |
TRG_ENDOCYTIC_2 | 513 | 516 | PF00928 | 0.428 |
TRG_ENDOCYTIC_2 | 529 | 532 | PF00928 | 0.429 |
TRG_ENDOCYTIC_2 | 566 | 569 | PF00928 | 0.368 |
TRG_ER_diArg_1 | 130 | 133 | PF00400 | 0.678 |
TRG_Pf-PMV_PEXEL_1 | 11 | 15 | PF00026 | 0.551 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8T6 | Leptomonas seymouri | 35% | 93% |
A0A0N1I8N2 | Leptomonas seymouri | 29% | 66% |
A0A0N1IGQ2 | Leptomonas seymouri | 34% | 92% |
A0A0N1P9P1 | Leptomonas seymouri | 36% | 76% |
A0A0N1PCA9 | Leptomonas seymouri | 34% | 88% |
A0A0N1PE91 | Leptomonas seymouri | 24% | 73% |
A0A1X0NJK2 | Trypanosomatidae | 31% | 86% |
A0A1X0NMT3 | Trypanosomatidae | 40% | 76% |
A0A1X0NWA6 | Trypanosomatidae | 30% | 75% |
A0A3S7WW41 | Leishmania donovani | 35% | 88% |
A0A3S7X463 | Leishmania donovani | 26% | 70% |
A4H3W4 | Leishmania braziliensis | 36% | 76% |
A4HE81 | Leishmania braziliensis | 35% | 92% |
A4HJ22 | Leishmania braziliensis | 31% | 69% |
A4HJ23 | Leishmania braziliensis | 38% | 100% |
A4HYW3 | Leishmania infantum | 35% | 88% |
A4I6K5 | Leishmania infantum | 26% | 70% |
A8MX76 | Homo sapiens | 28% | 95% |
C9ZY36 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 76% |
E8NHF1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
E8NHG7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 69% |
E8NHM8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
E8NHQ2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 100% |
E9AIH4 | Leishmania braziliensis | 35% | 88% |
E9AIH6 | Leishmania braziliensis | 27% | 100% |
E9AK26 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 82% |
E9AUR0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 88% |
E9AUR1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9B1J1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 70% |
P27730 | Schistosoma mansoni | 24% | 86% |
Q4Q6L7 | Leishmania major | 36% | 89% |
Q4Q6M0 | Leishmania major | 29% | 69% |
Q4Q6M2 | Leishmania major | 23% | 86% |
Q4Q6M3 | Leishmania major | 27% | 70% |
Q4QCS6 | Leishmania major | 36% | 88% |
V5D9Y2 | Trypanosoma cruzi | 36% | 77% |