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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: E9AYJ5
Term | Name | Level | Count |
---|---|---|---|
GO:0008152 | metabolic process | 1 | 4 |
GO:0032259 | methylation | 2 | 4 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 4 |
GO:0008168 | methyltransferase activity | 4 | 4 |
GO:0016740 | transferase activity | 2 | 4 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 4 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 202 | 206 | PF00656 | 0.412 |
CLV_C14_Caspase3-7 | 438 | 442 | PF00656 | 0.580 |
CLV_NRD_NRD_1 | 121 | 123 | PF00675 | 0.484 |
CLV_NRD_NRD_1 | 291 | 293 | PF00675 | 0.584 |
CLV_NRD_NRD_1 | 426 | 428 | PF00675 | 0.588 |
CLV_NRD_NRD_1 | 43 | 45 | PF00675 | 0.519 |
CLV_NRD_NRD_1 | 523 | 525 | PF00675 | 0.398 |
CLV_NRD_NRD_1 | 539 | 541 | PF00675 | 0.698 |
CLV_NRD_NRD_1 | 542 | 544 | PF00675 | 0.677 |
CLV_NRD_NRD_1 | 64 | 66 | PF00675 | 0.511 |
CLV_PCSK_FUR_1 | 289 | 293 | PF00082 | 0.487 |
CLV_PCSK_FUR_1 | 521 | 525 | PF00082 | 0.386 |
CLV_PCSK_FUR_1 | 540 | 544 | PF00082 | 0.700 |
CLV_PCSK_KEX2_1 | 121 | 123 | PF00082 | 0.425 |
CLV_PCSK_KEX2_1 | 291 | 293 | PF00082 | 0.588 |
CLV_PCSK_KEX2_1 | 43 | 45 | PF00082 | 0.551 |
CLV_PCSK_KEX2_1 | 523 | 525 | PF00082 | 0.388 |
CLV_PCSK_KEX2_1 | 539 | 541 | PF00082 | 0.574 |
CLV_PCSK_KEX2_1 | 542 | 544 | PF00082 | 0.566 |
CLV_PCSK_KEX2_1 | 551 | 553 | PF00082 | 0.541 |
CLV_PCSK_KEX2_1 | 64 | 66 | PF00082 | 0.511 |
CLV_PCSK_PC1ET2_1 | 551 | 553 | PF00082 | 0.590 |
CLV_PCSK_PC7_1 | 117 | 123 | PF00082 | 0.464 |
CLV_PCSK_SKI1_1 | 121 | 125 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 133 | 137 | PF00082 | 0.419 |
CLV_PCSK_SKI1_1 | 235 | 239 | PF00082 | 0.377 |
CLV_PCSK_SKI1_1 | 353 | 357 | PF00082 | 0.460 |
CLV_PCSK_SKI1_1 | 477 | 481 | PF00082 | 0.512 |
DEG_COP1_1 | 142 | 154 | PF00400 | 0.399 |
DEG_SCF_FBW7_1 | 466 | 471 | PF00400 | 0.401 |
DEG_SPOP_SBC_1 | 449 | 453 | PF00917 | 0.423 |
DOC_ANK_TNKS_1 | 291 | 298 | PF00023 | 0.379 |
DOC_MAPK_gen_1 | 481 | 488 | PF00069 | 0.376 |
DOC_MAPK_gen_1 | 49 | 58 | PF00069 | 0.283 |
DOC_PP2B_LxvP_1 | 347 | 350 | PF13499 | 0.417 |
DOC_PP2B_LxvP_1 | 5 | 8 | PF13499 | 0.628 |
DOC_USP7_MATH_1 | 150 | 154 | PF00917 | 0.645 |
DOC_USP7_MATH_1 | 299 | 303 | PF00917 | 0.631 |
DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.718 |
DOC_WW_Pin1_4 | 255 | 260 | PF00397 | 0.516 |
DOC_WW_Pin1_4 | 391 | 396 | PF00397 | 0.535 |
DOC_WW_Pin1_4 | 451 | 456 | PF00397 | 0.509 |
DOC_WW_Pin1_4 | 462 | 467 | PF00397 | 0.634 |
DOC_WW_Pin1_4 | 78 | 83 | PF00397 | 0.746 |
LIG_14-3-3_CanoR_1 | 30 | 35 | PF00244 | 0.530 |
LIG_14-3-3_CanoR_1 | 461 | 466 | PF00244 | 0.510 |
LIG_14-3-3_CanoR_1 | 51 | 57 | PF00244 | 0.500 |
LIG_14-3-3_CanoR_1 | 542 | 550 | PF00244 | 0.746 |
LIG_14-3-3_CanoR_1 | 71 | 79 | PF00244 | 0.419 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.713 |
LIG_BRCT_BRCA1_1 | 38 | 42 | PF00533 | 0.418 |
LIG_deltaCOP1_diTrp_1 | 510 | 519 | PF00928 | 0.342 |
LIG_FHA_1 | 100 | 106 | PF00498 | 0.634 |
LIG_FHA_1 | 21 | 27 | PF00498 | 0.575 |
LIG_FHA_1 | 252 | 258 | PF00498 | 0.521 |
LIG_FHA_1 | 406 | 412 | PF00498 | 0.376 |
LIG_FHA_1 | 442 | 448 | PF00498 | 0.397 |
LIG_FHA_1 | 465 | 471 | PF00498 | 0.520 |
LIG_FHA_1 | 545 | 551 | PF00498 | 0.619 |
LIG_FHA_2 | 200 | 206 | PF00498 | 0.559 |
LIG_LIR_Gen_1 | 205 | 215 | PF02991 | 0.421 |
LIG_LIR_Gen_1 | 376 | 384 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 174 | 180 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 205 | 211 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 39 | 45 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 50 | 56 | PF02991 | 0.391 |
LIG_PALB2_WD40_1 | 340 | 348 | PF16756 | 0.324 |
LIG_PTAP_UEV_1 | 151 | 156 | PF05743 | 0.347 |
LIG_REV1ctd_RIR_1 | 129 | 137 | PF16727 | 0.514 |
LIG_SH2_STAT5 | 170 | 173 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 25 | 28 | PF00017 | 0.464 |
LIG_SH2_STAT5 | 322 | 325 | PF00017 | 0.505 |
LIG_SH2_STAT5 | 34 | 37 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 358 | 361 | PF00017 | 0.471 |
LIG_SH2_STAT5 | 417 | 420 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 462 | 465 | PF00017 | 0.449 |
LIG_SH3_3 | 149 | 155 | PF00018 | 0.445 |
LIG_SH3_3 | 212 | 218 | PF00018 | 0.509 |
LIG_SH3_3 | 337 | 343 | PF00018 | 0.389 |
LIG_SH3_3 | 4 | 10 | PF00018 | 0.579 |
LIG_SH3_3 | 420 | 426 | PF00018 | 0.437 |
LIG_SH3_3 | 76 | 82 | PF00018 | 0.739 |
LIG_SUMO_SIM_anti_2 | 108 | 114 | PF11976 | 0.477 |
LIG_WW_3 | 424 | 428 | PF00397 | 0.513 |
MOD_CDK_SPK_2 | 451 | 456 | PF00069 | 0.509 |
MOD_CK1_1 | 140 | 146 | PF00069 | 0.664 |
MOD_CK1_1 | 204 | 210 | PF00069 | 0.456 |
MOD_CK1_1 | 258 | 264 | PF00069 | 0.525 |
MOD_CK1_1 | 304 | 310 | PF00069 | 0.497 |
MOD_CK1_1 | 330 | 336 | PF00069 | 0.616 |
MOD_CK1_1 | 396 | 402 | PF00069 | 0.440 |
MOD_CK1_1 | 451 | 457 | PF00069 | 0.595 |
MOD_CK1_1 | 72 | 78 | PF00069 | 0.642 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.677 |
MOD_GlcNHglycan | 152 | 155 | PF01048 | 0.451 |
MOD_GlcNHglycan | 185 | 188 | PF01048 | 0.422 |
MOD_GlcNHglycan | 19 | 23 | PF01048 | 0.524 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.554 |
MOD_GlcNHglycan | 260 | 263 | PF01048 | 0.388 |
MOD_GlcNHglycan | 268 | 271 | PF01048 | 0.370 |
MOD_GlcNHglycan | 301 | 304 | PF01048 | 0.592 |
MOD_GlcNHglycan | 306 | 309 | PF01048 | 0.635 |
MOD_GlcNHglycan | 396 | 399 | PF01048 | 0.655 |
MOD_GlcNHglycan | 532 | 535 | PF01048 | 0.597 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.683 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.606 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.530 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.513 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.553 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.633 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.392 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.266 |
MOD_GSK3_1 | 460 | 467 | PF00069 | 0.669 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.586 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.570 |
MOD_LATS_1 | 119 | 125 | PF00433 | 0.461 |
MOD_N-GLC_1 | 138 | 143 | PF02516 | 0.533 |
MOD_N-GLC_1 | 222 | 227 | PF02516 | 0.441 |
MOD_NEK2_1 | 24 | 29 | PF00069 | 0.510 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.440 |
MOD_NEK2_1 | 327 | 332 | PF00069 | 0.558 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.313 |
MOD_NEK2_1 | 409 | 414 | PF00069 | 0.346 |
MOD_NEK2_1 | 450 | 455 | PF00069 | 0.503 |
MOD_NEK2_1 | 460 | 465 | PF00069 | 0.604 |
MOD_PIKK_1 | 121 | 127 | PF00454 | 0.475 |
MOD_PIKK_1 | 213 | 219 | PF00454 | 0.506 |
MOD_PIKK_1 | 80 | 86 | PF00454 | 0.594 |
MOD_PKA_1 | 121 | 127 | PF00069 | 0.475 |
MOD_PKA_2 | 121 | 127 | PF00069 | 0.481 |
MOD_PKA_2 | 460 | 466 | PF00069 | 0.493 |
MOD_PKA_2 | 70 | 76 | PF00069 | 0.470 |
MOD_Plk_1 | 107 | 113 | PF00069 | 0.393 |
MOD_Plk_1 | 204 | 210 | PF00069 | 0.430 |
MOD_Plk_1 | 36 | 42 | PF00069 | 0.423 |
MOD_Plk_2-3 | 435 | 441 | PF00069 | 0.405 |
MOD_Plk_4 | 107 | 113 | PF00069 | 0.516 |
MOD_Plk_4 | 20 | 26 | PF00069 | 0.641 |
MOD_Plk_4 | 204 | 210 | PF00069 | 0.459 |
MOD_Plk_4 | 260 | 266 | PF00069 | 0.483 |
MOD_Plk_4 | 322 | 328 | PF00069 | 0.674 |
MOD_Plk_4 | 354 | 360 | PF00069 | 0.521 |
MOD_Plk_4 | 36 | 42 | PF00069 | 0.327 |
MOD_Plk_4 | 373 | 379 | PF00069 | 0.196 |
MOD_ProDKin_1 | 255 | 261 | PF00069 | 0.512 |
MOD_ProDKin_1 | 391 | 397 | PF00069 | 0.533 |
MOD_ProDKin_1 | 451 | 457 | PF00069 | 0.505 |
MOD_ProDKin_1 | 462 | 468 | PF00069 | 0.636 |
MOD_ProDKin_1 | 78 | 84 | PF00069 | 0.746 |
TRG_DiLeu_LyEn_5 | 192 | 197 | PF01217 | 0.392 |
TRG_ENDOCYTIC_2 | 505 | 508 | PF00928 | 0.462 |
TRG_ER_diArg_1 | 121 | 123 | PF00400 | 0.484 |
TRG_ER_diArg_1 | 289 | 292 | PF00400 | 0.592 |
TRG_ER_diArg_1 | 400 | 403 | PF00400 | 0.437 |
TRG_ER_diArg_1 | 42 | 44 | PF00400 | 0.550 |
TRG_ER_diArg_1 | 520 | 523 | PF00400 | 0.393 |
TRG_ER_diArg_1 | 538 | 540 | PF00400 | 0.531 |
TRG_NLS_Bipartite_1 | 539 | 555 | PF00514 | 0.574 |
TRG_NLS_MonoExtC_3 | 550 | 556 | PF00514 | 0.678 |
TRG_Pf-PMV_PEXEL_1 | 121 | 125 | PF00026 | 0.508 |
TRG_Pf-PMV_PEXEL_1 | 169 | 173 | PF00026 | 0.456 |
TRG_Pf-PMV_PEXEL_1 | 43 | 47 | PF00026 | 0.418 |
TRG_Pf-PMV_PEXEL_1 | 477 | 482 | PF00026 | 0.521 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IIL5 | Leptomonas seymouri | 48% | 97% |
A0A1X0P8D1 | Trypanosomatidae | 31% | 100% |
A0A3S7X044 | Leishmania donovani | 89% | 100% |
A0A422N0J7 | Trypanosoma rangeli | 32% | 100% |
A4HF59 | Leishmania braziliensis | 75% | 100% |
A4I2E3 | Leishmania infantum | 89% | 100% |
C9ZX64 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
Q4Q8X7 | Leishmania major | 87% | 100% |
V5BJ25 | Trypanosoma cruzi | 31% | 100% |