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: A4HF59
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 | 439 | 443 | PF00656 | 0.552 |
CLV_NRD_NRD_1 | 125 | 127 | PF00675 | 0.479 |
CLV_NRD_NRD_1 | 47 | 49 | PF00675 | 0.520 |
CLV_NRD_NRD_1 | 523 | 525 | PF00675 | 0.397 |
CLV_NRD_NRD_1 | 68 | 70 | PF00675 | 0.497 |
CLV_PCSK_FUR_1 | 521 | 525 | PF00082 | 0.385 |
CLV_PCSK_KEX2_1 | 118 | 120 | PF00082 | 0.443 |
CLV_PCSK_KEX2_1 | 125 | 127 | PF00082 | 0.420 |
CLV_PCSK_KEX2_1 | 47 | 49 | PF00082 | 0.551 |
CLV_PCSK_KEX2_1 | 523 | 525 | PF00082 | 0.387 |
CLV_PCSK_KEX2_1 | 551 | 553 | PF00082 | 0.543 |
CLV_PCSK_KEX2_1 | 68 | 70 | PF00082 | 0.497 |
CLV_PCSK_PC1ET2_1 | 118 | 120 | PF00082 | 0.405 |
CLV_PCSK_PC1ET2_1 | 551 | 553 | PF00082 | 0.592 |
CLV_PCSK_SKI1_1 | 354 | 358 | PF00082 | 0.331 |
CLV_PCSK_SKI1_1 | 477 | 481 | PF00082 | 0.529 |
CLV_PCSK_SKI1_1 | 88 | 92 | PF00082 | 0.611 |
CLV_PCSK_SKI1_1 | 9 | 13 | PF00082 | 0.665 |
DEG_APCC_DBOX_1 | 353 | 361 | PF00400 | 0.381 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.557 |
DEG_SPOP_SBC_1 | 246 | 250 | PF00917 | 0.381 |
DEG_SPOP_SBC_1 | 393 | 397 | PF00917 | 0.381 |
DEG_SPOP_SBC_1 | 450 | 454 | PF00917 | 0.433 |
DEG_SPOP_SBC_1 | 467 | 471 | PF00917 | 0.406 |
DOC_CYCLIN_RxL_1 | 474 | 482 | PF00134 | 0.353 |
DOC_CYCLIN_yCln2_LP_2 | 11 | 14 | PF00134 | 0.439 |
DOC_PP2B_LxvP_1 | 11 | 14 | PF13499 | 0.567 |
DOC_PP2B_LxvP_1 | 348 | 351 | PF13499 | 0.506 |
DOC_USP7_MATH_1 | 140 | 144 | PF00917 | 0.423 |
DOC_USP7_MATH_1 | 154 | 158 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 247 | 251 | PF00917 | 0.421 |
DOC_USP7_MATH_1 | 303 | 307 | PF00917 | 0.530 |
DOC_USP7_MATH_1 | 327 | 331 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 393 | 397 | PF00917 | 0.449 |
DOC_USP7_MATH_1 | 460 | 464 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 84 | 88 | PF00917 | 0.697 |
DOC_WW_Pin1_4 | 323 | 328 | PF00397 | 0.563 |
DOC_WW_Pin1_4 | 452 | 457 | PF00397 | 0.531 |
DOC_WW_Pin1_4 | 463 | 468 | PF00397 | 0.655 |
DOC_WW_Pin1_4 | 469 | 474 | PF00397 | 0.642 |
DOC_WW_Pin1_4 | 71 | 76 | PF00397 | 0.571 |
DOC_WW_Pin1_4 | 82 | 87 | PF00397 | 0.724 |
LIG_14-3-3_CanoR_1 | 141 | 146 | PF00244 | 0.601 |
LIG_14-3-3_CanoR_1 | 34 | 39 | PF00244 | 0.522 |
LIG_14-3-3_CanoR_1 | 354 | 360 | PF00244 | 0.381 |
LIG_14-3-3_CanoR_1 | 428 | 437 | PF00244 | 0.487 |
LIG_14-3-3_CanoR_1 | 543 | 553 | PF00244 | 0.745 |
LIG_14-3-3_CanoR_1 | 55 | 65 | PF00244 | 0.491 |
LIG_14-3-3_CanoR_1 | 69 | 75 | PF00244 | 0.461 |
LIG_BIR_III_2 | 324 | 328 | PF00653 | 0.539 |
LIG_BRCT_BRCA1_1 | 42 | 46 | PF00533 | 0.413 |
LIG_deltaCOP1_diTrp_1 | 510 | 519 | PF00928 | 0.343 |
LIG_FHA_1 | 104 | 110 | PF00498 | 0.627 |
LIG_FHA_1 | 407 | 413 | PF00498 | 0.365 |
LIG_FHA_1 | 430 | 436 | PF00498 | 0.471 |
LIG_FHA_1 | 443 | 449 | PF00498 | 0.393 |
LIG_FHA_1 | 545 | 551 | PF00498 | 0.602 |
LIG_FHA_2 | 253 | 259 | PF00498 | 0.477 |
LIG_FHA_2 | 332 | 338 | PF00498 | 0.381 |
LIG_LIR_Gen_1 | 134 | 142 | PF02991 | 0.312 |
LIG_LIR_Gen_1 | 209 | 219 | PF02991 | 0.478 |
LIG_LIR_Gen_1 | 229 | 240 | PF02991 | 0.371 |
LIG_LIR_Gen_1 | 276 | 287 | PF02991 | 0.414 |
LIG_LIR_Gen_1 | 377 | 385 | PF02991 | 0.492 |
LIG_LIR_Gen_1 | 510 | 520 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 134 | 139 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 178 | 184 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 209 | 215 | PF02991 | 0.509 |
LIG_LIR_Nem_3 | 229 | 235 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 276 | 282 | PF02991 | 0.396 |
LIG_LIR_Nem_3 | 43 | 49 | PF02991 | 0.352 |
LIG_LIR_Nem_3 | 500 | 505 | PF02991 | 0.442 |
LIG_NRBOX | 263 | 269 | PF00104 | 0.381 |
LIG_PALB2_WD40_1 | 341 | 349 | PF16756 | 0.436 |
LIG_PTAP_UEV_1 | 155 | 160 | PF05743 | 0.340 |
LIG_SH2_NCK_1 | 232 | 236 | PF00017 | 0.381 |
LIG_SH2_SRC | 232 | 235 | PF00017 | 0.381 |
LIG_SH2_STAP1 | 240 | 244 | PF00017 | 0.488 |
LIG_SH2_STAP1 | 475 | 479 | PF00017 | 0.361 |
LIG_SH2_STAP1 | 66 | 70 | PF00017 | 0.336 |
LIG_SH2_STAT5 | 174 | 177 | PF00017 | 0.492 |
LIG_SH2_STAT5 | 29 | 32 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 359 | 362 | PF00017 | 0.531 |
LIG_SH2_STAT5 | 38 | 41 | PF00017 | 0.346 |
LIG_SH2_STAT5 | 418 | 421 | PF00017 | 0.310 |
LIG_SH3_3 | 153 | 159 | PF00018 | 0.426 |
LIG_SH3_3 | 216 | 222 | PF00018 | 0.531 |
LIG_SH3_3 | 241 | 247 | PF00018 | 0.381 |
LIG_SH3_3 | 338 | 344 | PF00018 | 0.451 |
LIG_SH3_3 | 421 | 427 | PF00018 | 0.424 |
LIG_SH3_3 | 83 | 89 | PF00018 | 0.722 |
LIG_SUMO_SIM_par_1 | 198 | 204 | PF11976 | 0.381 |
LIG_UBA3_1 | 263 | 270 | PF00899 | 0.381 |
LIG_WW_3 | 425 | 429 | PF00397 | 0.492 |
MOD_CDC14_SPxK_1 | 85 | 88 | PF00782 | 0.574 |
MOD_CDK_SPK_2 | 452 | 457 | PF00069 | 0.531 |
MOD_CDK_SPxK_1 | 82 | 88 | PF00069 | 0.725 |
MOD_CK1_1 | 144 | 150 | PF00069 | 0.630 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.490 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.371 |
MOD_CK1_1 | 239 | 245 | PF00069 | 0.443 |
MOD_CK1_1 | 248 | 254 | PF00069 | 0.419 |
MOD_CK1_1 | 271 | 277 | PF00069 | 0.474 |
MOD_CK1_1 | 326 | 332 | PF00069 | 0.532 |
MOD_CK1_1 | 452 | 458 | PF00069 | 0.621 |
MOD_CK1_1 | 463 | 469 | PF00069 | 0.609 |
MOD_CK1_1 | 76 | 82 | PF00069 | 0.639 |
MOD_CK2_1 | 252 | 258 | PF00069 | 0.381 |
MOD_CK2_1 | 270 | 276 | PF00069 | 0.353 |
MOD_CK2_1 | 331 | 337 | PF00069 | 0.381 |
MOD_GlcNHglycan | 156 | 159 | PF01048 | 0.440 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.247 |
MOD_GlcNHglycan | 228 | 231 | PF01048 | 0.331 |
MOD_GlcNHglycan | 23 | 27 | PF01048 | 0.519 |
MOD_GlcNHglycan | 244 | 247 | PF01048 | 0.331 |
MOD_GlcNHglycan | 250 | 253 | PF01048 | 0.249 |
MOD_GlcNHglycan | 305 | 308 | PF01048 | 0.302 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.346 |
MOD_GlcNHglycan | 397 | 400 | PF01048 | 0.649 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.647 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.473 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.690 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.662 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.635 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.531 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.525 |
MOD_GSK3_1 | 242 | 249 | PF00069 | 0.437 |
MOD_GSK3_1 | 268 | 275 | PF00069 | 0.388 |
MOD_GSK3_1 | 308 | 315 | PF00069 | 0.490 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.502 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.477 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.482 |
MOD_GSK3_1 | 462 | 469 | PF00069 | 0.716 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.585 |
MOD_N-GLC_1 | 102 | 107 | PF02516 | 0.412 |
MOD_N-GLC_1 | 242 | 247 | PF02516 | 0.201 |
MOD_N-GLC_1 | 71 | 76 | PF02516 | 0.595 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.535 |
MOD_NEK2_1 | 145 | 150 | PF00069 | 0.628 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.452 |
MOD_NEK2_1 | 268 | 273 | PF00069 | 0.425 |
MOD_NEK2_1 | 28 | 33 | PF00069 | 0.507 |
MOD_NEK2_1 | 40 | 45 | PF00069 | 0.308 |
MOD_NEK2_1 | 451 | 456 | PF00069 | 0.516 |
MOD_NEK2_1 | 461 | 466 | PF00069 | 0.652 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.412 |
MOD_NEK2_2 | 131 | 136 | PF00069 | 0.360 |
MOD_NEK2_2 | 400 | 405 | PF00069 | 0.313 |
MOD_PIKK_1 | 217 | 223 | PF00454 | 0.531 |
MOD_PIKK_1 | 96 | 102 | PF00454 | 0.580 |
MOD_PKA_2 | 140 | 146 | PF00069 | 0.549 |
MOD_PKA_2 | 400 | 406 | PF00069 | 0.305 |
MOD_Plk_1 | 1 | 7 | PF00069 | 0.594 |
MOD_Plk_1 | 208 | 214 | PF00069 | 0.472 |
MOD_Plk_1 | 40 | 46 | PF00069 | 0.419 |
MOD_Plk_4 | 131 | 137 | PF00069 | 0.313 |
MOD_Plk_4 | 208 | 214 | PF00069 | 0.492 |
MOD_Plk_4 | 24 | 30 | PF00069 | 0.636 |
MOD_Plk_4 | 262 | 268 | PF00069 | 0.472 |
MOD_Plk_4 | 355 | 361 | PF00069 | 0.582 |
MOD_Plk_4 | 374 | 380 | PF00069 | 0.358 |
MOD_ProDKin_1 | 323 | 329 | PF00069 | 0.563 |
MOD_ProDKin_1 | 452 | 458 | PF00069 | 0.531 |
MOD_ProDKin_1 | 463 | 469 | PF00069 | 0.654 |
MOD_ProDKin_1 | 71 | 77 | PF00069 | 0.581 |
MOD_ProDKin_1 | 82 | 88 | PF00069 | 0.725 |
TRG_DiLeu_BaEn_1 | 258 | 263 | PF01217 | 0.381 |
TRG_DiLeu_BaLyEn_6 | 196 | 201 | PF01217 | 0.381 |
TRG_ENDOCYTIC_2 | 232 | 235 | PF00928 | 0.428 |
TRG_ENDOCYTIC_2 | 505 | 508 | PF00928 | 0.461 |
TRG_ER_diArg_1 | 125 | 127 | PF00400 | 0.479 |
TRG_ER_diArg_1 | 293 | 296 | PF00400 | 0.529 |
TRG_ER_diArg_1 | 46 | 48 | PF00400 | 0.551 |
TRG_ER_diArg_1 | 520 | 523 | PF00400 | 0.392 |
TRG_ER_diArg_1 | 68 | 70 | PF00400 | 0.384 |
TRG_NLS_MonoExtC_3 | 550 | 556 | PF00514 | 0.677 |
TRG_Pf-PMV_PEXEL_1 | 125 | 129 | PF00026 | 0.501 |
TRG_Pf-PMV_PEXEL_1 | 173 | 177 | PF00026 | 0.331 |
TRG_Pf-PMV_PEXEL_1 | 438 | 442 | PF00026 | 0.570 |
TRG_Pf-PMV_PEXEL_1 | 47 | 51 | PF00026 | 0.421 |
TRG_Pf-PMV_PEXEL_1 | 477 | 482 | PF00026 | 0.542 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IIL5 | Leptomonas seymouri | 48% | 97% |
A0A1X0P8D1 | Trypanosomatidae | 31% | 100% |
A0A3S7X044 | Leishmania donovani | 75% | 100% |
A0A422N0J7 | Trypanosoma rangeli | 34% | 100% |
A4I2E3 | Leishmania infantum | 75% | 100% |
C9ZX64 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
E9AYJ5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 100% |
Q4Q8X7 | Leishmania major | 75% | 100% |
V5BJ25 | Trypanosoma cruzi | 32% | 100% |