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: A0A3S7X044
Term | Name | Level | Count |
---|---|---|---|
GO:0008152 | metabolic process | 1 | 5 |
GO:0032259 | methylation | 2 | 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 5 |
GO:0008168 | methyltransferase activity | 4 | 5 |
GO:0016740 | transferase activity | 2 | 5 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 5 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 326 | 330 | PF00656 | 0.570 |
CLV_NRD_NRD_1 | 121 | 123 | PF00675 | 0.531 |
CLV_NRD_NRD_1 | 291 | 293 | PF00675 | 0.355 |
CLV_NRD_NRD_1 | 427 | 429 | PF00675 | 0.622 |
CLV_NRD_NRD_1 | 43 | 45 | PF00675 | 0.550 |
CLV_NRD_NRD_1 | 524 | 526 | PF00675 | 0.450 |
CLV_NRD_NRD_1 | 540 | 542 | PF00675 | 0.729 |
CLV_NRD_NRD_1 | 543 | 545 | PF00675 | 0.718 |
CLV_NRD_NRD_1 | 64 | 66 | PF00675 | 0.571 |
CLV_PCSK_FUR_1 | 289 | 293 | PF00082 | 0.330 |
CLV_PCSK_FUR_1 | 522 | 526 | PF00082 | 0.457 |
CLV_PCSK_FUR_1 | 541 | 545 | PF00082 | 0.732 |
CLV_PCSK_KEX2_1 | 121 | 123 | PF00082 | 0.487 |
CLV_PCSK_KEX2_1 | 291 | 293 | PF00082 | 0.357 |
CLV_PCSK_KEX2_1 | 43 | 45 | PF00082 | 0.555 |
CLV_PCSK_KEX2_1 | 524 | 526 | PF00082 | 0.458 |
CLV_PCSK_KEX2_1 | 540 | 542 | PF00082 | 0.635 |
CLV_PCSK_KEX2_1 | 543 | 545 | PF00082 | 0.628 |
CLV_PCSK_KEX2_1 | 552 | 554 | PF00082 | 0.595 |
CLV_PCSK_KEX2_1 | 64 | 66 | PF00082 | 0.571 |
CLV_PCSK_KEX2_1 | 92 | 94 | PF00082 | 0.726 |
CLV_PCSK_PC1ET2_1 | 552 | 554 | PF00082 | 0.648 |
CLV_PCSK_PC1ET2_1 | 92 | 94 | PF00082 | 0.726 |
CLV_PCSK_PC7_1 | 117 | 123 | PF00082 | 0.515 |
CLV_PCSK_SKI1_1 | 121 | 125 | PF00082 | 0.420 |
CLV_PCSK_SKI1_1 | 354 | 358 | PF00082 | 0.343 |
CLV_PCSK_SKI1_1 | 478 | 482 | PF00082 | 0.579 |
DEG_SPOP_SBC_1 | 450 | 454 | PF00917 | 0.553 |
DOC_MAPK_DCC_7 | 149 | 158 | PF00069 | 0.408 |
DOC_MAPK_gen_1 | 482 | 489 | PF00069 | 0.494 |
DOC_MAPK_RevD_3 | 77 | 93 | PF00069 | 0.651 |
DOC_PP2B_LxvP_1 | 348 | 351 | PF13499 | 0.544 |
DOC_PP2B_LxvP_1 | 5 | 8 | PF13499 | 0.776 |
DOC_USP7_MATH_1 | 246 | 250 | PF00917 | 0.480 |
DOC_USP7_MATH_1 | 323 | 327 | PF00917 | 0.575 |
DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.745 |
DOC_WW_Pin1_4 | 149 | 154 | PF00397 | 0.487 |
DOC_WW_Pin1_4 | 328 | 333 | PF00397 | 0.568 |
DOC_WW_Pin1_4 | 392 | 397 | PF00397 | 0.637 |
DOC_WW_Pin1_4 | 452 | 457 | PF00397 | 0.555 |
DOC_WW_Pin1_4 | 465 | 470 | PF00397 | 0.680 |
DOC_WW_Pin1_4 | 6 | 11 | PF00397 | 0.739 |
DOC_WW_Pin1_4 | 78 | 83 | PF00397 | 0.759 |
LIG_14-3-3_CanoR_1 | 30 | 35 | PF00244 | 0.533 |
LIG_14-3-3_CanoR_1 | 463 | 469 | PF00244 | 0.628 |
LIG_14-3-3_CanoR_1 | 51 | 61 | PF00244 | 0.552 |
LIG_14-3-3_CanoR_1 | 543 | 551 | PF00244 | 0.759 |
LIG_14-3-3_CanoR_1 | 71 | 79 | PF00244 | 0.413 |
LIG_14-3-3_CanoR_1 | 84 | 91 | PF00244 | 0.743 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.713 |
LIG_BRCT_BRCA1_1 | 128 | 132 | PF00533 | 0.476 |
LIG_BRCT_BRCA1_1 | 38 | 42 | PF00533 | 0.476 |
LIG_deltaCOP1_diTrp_1 | 511 | 520 | PF00928 | 0.412 |
LIG_EVH1_1 | 7 | 11 | PF00568 | 0.656 |
LIG_FHA_1 | 100 | 106 | PF00498 | 0.696 |
LIG_FHA_1 | 21 | 27 | PF00498 | 0.615 |
LIG_FHA_1 | 252 | 258 | PF00498 | 0.530 |
LIG_FHA_1 | 407 | 413 | PF00498 | 0.436 |
LIG_FHA_1 | 443 | 449 | PF00498 | 0.526 |
LIG_FHA_1 | 466 | 472 | PF00498 | 0.629 |
LIG_FHA_1 | 546 | 552 | PF00498 | 0.759 |
LIG_FHA_2 | 12 | 18 | PF00498 | 0.697 |
LIG_LIR_Gen_1 | 207 | 215 | PF02991 | 0.595 |
LIG_LIR_Gen_1 | 225 | 234 | PF02991 | 0.391 |
LIG_LIR_Gen_1 | 377 | 385 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 174 | 180 | PF02991 | 0.556 |
LIG_LIR_Nem_3 | 207 | 211 | PF02991 | 0.549 |
LIG_LIR_Nem_3 | 39 | 45 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 501 | 506 | PF02991 | 0.511 |
LIG_MLH1_MIPbox_1 | 128 | 132 | PF16413 | 0.476 |
LIG_PALB2_WD40_1 | 341 | 349 | PF16756 | 0.482 |
LIG_REV1ctd_RIR_1 | 129 | 135 | PF16727 | 0.545 |
LIG_SH2_STAT5 | 170 | 173 | PF00017 | 0.534 |
LIG_SH2_STAT5 | 25 | 28 | PF00017 | 0.513 |
LIG_SH2_STAT5 | 34 | 37 | PF00017 | 0.342 |
LIG_SH2_STAT5 | 359 | 362 | PF00017 | 0.562 |
LIG_SH2_STAT5 | 418 | 421 | PF00017 | 0.377 |
LIG_SH2_STAT5 | 470 | 473 | PF00017 | 0.517 |
LIG_SH3_3 | 147 | 153 | PF00018 | 0.593 |
LIG_SH3_3 | 212 | 218 | PF00018 | 0.534 |
LIG_SH3_3 | 338 | 344 | PF00018 | 0.498 |
LIG_SH3_3 | 386 | 392 | PF00018 | 0.371 |
LIG_SH3_3 | 421 | 427 | PF00018 | 0.575 |
LIG_SH3_3 | 5 | 11 | PF00018 | 0.697 |
LIG_SH3_3 | 76 | 82 | PF00018 | 0.756 |
LIG_SUMO_SIM_anti_2 | 108 | 114 | PF11976 | 0.528 |
LIG_WW_3 | 425 | 429 | PF00397 | 0.643 |
MOD_CDC14_SPxK_1 | 81 | 84 | PF00782 | 0.721 |
MOD_CDK_SPK_2 | 452 | 457 | PF00069 | 0.555 |
MOD_CDK_SPxK_1 | 78 | 84 | PF00069 | 0.762 |
MOD_CK1_1 | 140 | 146 | PF00069 | 0.707 |
MOD_CK1_1 | 201 | 207 | PF00069 | 0.512 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.593 |
MOD_CK1_1 | 330 | 336 | PF00069 | 0.548 |
MOD_CK1_1 | 452 | 458 | PF00069 | 0.599 |
MOD_CK2_1 | 11 | 17 | PF00069 | 0.748 |
MOD_CK2_1 | 82 | 88 | PF00069 | 0.764 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.722 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.497 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.571 |
MOD_GlcNHglycan | 203 | 206 | PF01048 | 0.389 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.362 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.345 |
MOD_GlcNHglycan | 260 | 263 | PF01048 | 0.246 |
MOD_GlcNHglycan | 268 | 271 | PF01048 | 0.174 |
MOD_GlcNHglycan | 301 | 304 | PF01048 | 0.342 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.377 |
MOD_GlcNHglycan | 397 | 400 | PF01048 | 0.655 |
MOD_GlcNHglycan | 533 | 536 | PF01048 | 0.654 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.519 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.711 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.653 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.704 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.586 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.562 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.561 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.446 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.555 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.586 |
MOD_GSK3_1 | 461 | 468 | PF00069 | 0.655 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.633 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.649 |
MOD_LATS_1 | 119 | 125 | PF00433 | 0.511 |
MOD_N-GLC_1 | 138 | 143 | PF02516 | 0.641 |
MOD_N-GLC_1 | 222 | 227 | PF02516 | 0.341 |
MOD_NEK2_1 | 198 | 203 | PF00069 | 0.519 |
MOD_NEK2_1 | 24 | 29 | PF00069 | 0.560 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.531 |
MOD_NEK2_1 | 312 | 317 | PF00069 | 0.593 |
MOD_NEK2_1 | 327 | 332 | PF00069 | 0.490 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.381 |
MOD_NEK2_1 | 419 | 424 | PF00069 | 0.441 |
MOD_NEK2_1 | 451 | 456 | PF00069 | 0.546 |
MOD_NEK2_1 | 461 | 466 | PF00069 | 0.635 |
MOD_PIKK_1 | 121 | 127 | PF00454 | 0.528 |
MOD_PIKK_1 | 213 | 219 | PF00454 | 0.562 |
MOD_PIKK_1 | 92 | 98 | PF00454 | 0.726 |
MOD_PKA_1 | 121 | 127 | PF00069 | 0.528 |
MOD_PKA_1 | 92 | 98 | PF00069 | 0.715 |
MOD_PKA_2 | 121 | 127 | PF00069 | 0.531 |
MOD_PKA_2 | 246 | 252 | PF00069 | 0.433 |
MOD_PKA_2 | 462 | 468 | PF00069 | 0.658 |
MOD_PKA_2 | 53 | 59 | PF00069 | 0.537 |
MOD_PKA_2 | 70 | 76 | PF00069 | 0.518 |
MOD_PKA_2 | 92 | 98 | PF00069 | 0.649 |
MOD_Plk_1 | 107 | 113 | PF00069 | 0.504 |
MOD_Plk_1 | 296 | 302 | PF00069 | 0.502 |
MOD_Plk_1 | 323 | 329 | PF00069 | 0.433 |
MOD_Plk_1 | 36 | 42 | PF00069 | 0.482 |
MOD_Plk_4 | 107 | 113 | PF00069 | 0.555 |
MOD_Plk_4 | 20 | 26 | PF00069 | 0.655 |
MOD_Plk_4 | 204 | 210 | PF00069 | 0.534 |
MOD_Plk_4 | 260 | 266 | PF00069 | 0.580 |
MOD_Plk_4 | 296 | 302 | PF00069 | 0.429 |
MOD_Plk_4 | 355 | 361 | PF00069 | 0.593 |
MOD_Plk_4 | 36 | 42 | PF00069 | 0.413 |
MOD_Plk_4 | 374 | 380 | PF00069 | 0.393 |
MOD_ProDKin_1 | 149 | 155 | PF00069 | 0.473 |
MOD_ProDKin_1 | 328 | 334 | PF00069 | 0.568 |
MOD_ProDKin_1 | 392 | 398 | PF00069 | 0.634 |
MOD_ProDKin_1 | 452 | 458 | PF00069 | 0.553 |
MOD_ProDKin_1 | 465 | 471 | PF00069 | 0.676 |
MOD_ProDKin_1 | 6 | 12 | PF00069 | 0.738 |
MOD_ProDKin_1 | 78 | 84 | PF00069 | 0.762 |
MOD_SUMO_rev_2 | 141 | 151 | PF00179 | 0.615 |
TRG_DiLeu_BaEn_1 | 296 | 301 | PF01217 | 0.377 |
TRG_DiLeu_LyEn_5 | 192 | 197 | PF01217 | 0.530 |
TRG_ENDOCYTIC_2 | 228 | 231 | PF00928 | 0.488 |
TRG_ENDOCYTIC_2 | 506 | 509 | PF00928 | 0.512 |
TRG_ER_diArg_1 | 121 | 123 | PF00400 | 0.531 |
TRG_ER_diArg_1 | 289 | 292 | PF00400 | 0.560 |
TRG_ER_diArg_1 | 401 | 404 | PF00400 | 0.621 |
TRG_ER_diArg_1 | 42 | 44 | PF00400 | 0.565 |
TRG_ER_diArg_1 | 521 | 524 | PF00400 | 0.453 |
TRG_ER_diArg_1 | 539 | 541 | PF00400 | 0.591 |
TRG_NLS_Bipartite_1 | 540 | 556 | PF00514 | 0.679 |
TRG_NLS_MonoExtC_3 | 551 | 557 | PF00514 | 0.722 |
TRG_Pf-PMV_PEXEL_1 | 121 | 125 | PF00026 | 0.533 |
TRG_Pf-PMV_PEXEL_1 | 169 | 173 | PF00026 | 0.362 |
TRG_Pf-PMV_PEXEL_1 | 43 | 47 | PF00026 | 0.483 |
TRG_Pf-PMV_PEXEL_1 | 478 | 483 | PF00026 | 0.571 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IIL5 | Leptomonas seymouri | 47% | 97% |
A0A1X0P8D1 | Trypanosomatidae | 31% | 100% |
A0A422N0J7 | Trypanosoma rangeli | 34% | 100% |
A4HF59 | Leishmania braziliensis | 75% | 100% |
A4I2E3 | Leishmania infantum | 99% | 100% |
C9ZX64 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
E9AYJ5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4Q8X7 | Leishmania major | 91% | 100% |
V5BJ25 | Trypanosoma cruzi | 32% | 100% |