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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HFF0
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 3 |
GO:0016787 | hydrolase activity | 2 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 232 | 234 | PF00675 | 0.422 |
CLV_NRD_NRD_1 | 343 | 345 | PF00675 | 0.447 |
CLV_NRD_NRD_1 | 365 | 367 | PF00675 | 0.471 |
CLV_NRD_NRD_1 | 375 | 377 | PF00675 | 0.386 |
CLV_NRD_NRD_1 | 413 | 415 | PF00675 | 0.584 |
CLV_NRD_NRD_1 | 468 | 470 | PF00675 | 0.587 |
CLV_NRD_NRD_1 | 475 | 477 | PF00675 | 0.504 |
CLV_NRD_NRD_1 | 485 | 487 | PF00675 | 0.409 |
CLV_PCSK_FUR_1 | 483 | 487 | PF00082 | 0.375 |
CLV_PCSK_KEX2_1 | 232 | 234 | PF00082 | 0.422 |
CLV_PCSK_KEX2_1 | 343 | 345 | PF00082 | 0.450 |
CLV_PCSK_KEX2_1 | 365 | 367 | PF00082 | 0.444 |
CLV_PCSK_KEX2_1 | 375 | 377 | PF00082 | 0.325 |
CLV_PCSK_KEX2_1 | 413 | 415 | PF00082 | 0.584 |
CLV_PCSK_KEX2_1 | 468 | 470 | PF00082 | 0.587 |
CLV_PCSK_KEX2_1 | 475 | 477 | PF00082 | 0.504 |
CLV_PCSK_KEX2_1 | 485 | 487 | PF00082 | 0.409 |
CLV_PCSK_PC1ET2_1 | 485 | 487 | PF00082 | 0.451 |
CLV_PCSK_SKI1_1 | 315 | 319 | PF00082 | 0.465 |
CLV_PCSK_SKI1_1 | 344 | 348 | PF00082 | 0.364 |
CLV_PCSK_SKI1_1 | 375 | 379 | PF00082 | 0.422 |
CLV_PCSK_SKI1_1 | 469 | 473 | PF00082 | 0.680 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.586 |
DEG_SPOP_SBC_1 | 125 | 129 | PF00917 | 0.396 |
DOC_CKS1_1 | 252 | 257 | PF01111 | 0.478 |
DOC_CYCLIN_RxL_1 | 340 | 351 | PF00134 | 0.449 |
DOC_CYCLIN_RxL_1 | 372 | 381 | PF00134 | 0.464 |
DOC_CYCLIN_yCln2_LP_2 | 252 | 258 | PF00134 | 0.441 |
DOC_MAPK_gen_1 | 170 | 180 | PF00069 | 0.362 |
DOC_MAPK_gen_1 | 340 | 350 | PF00069 | 0.428 |
DOC_MAPK_gen_1 | 365 | 373 | PF00069 | 0.500 |
DOC_MAPK_gen_1 | 413 | 420 | PF00069 | 0.510 |
DOC_MAPK_gen_1 | 462 | 472 | PF00069 | 0.641 |
DOC_MAPK_gen_1 | 81 | 90 | PF00069 | 0.537 |
DOC_MAPK_MEF2A_6 | 343 | 350 | PF00069 | 0.435 |
DOC_MAPK_NFAT4_5 | 343 | 351 | PF00069 | 0.476 |
DOC_MAPK_RevD_3 | 217 | 233 | PF00069 | 0.420 |
DOC_PP1_RVXF_1 | 466 | 473 | PF00149 | 0.567 |
DOC_PP4_FxxP_1 | 441 | 444 | PF00568 | 0.504 |
DOC_PP4_FxxP_1 | 97 | 100 | PF00568 | 0.484 |
DOC_USP7_MATH_1 | 158 | 162 | PF00917 | 0.495 |
DOC_USP7_MATH_1 | 186 | 190 | PF00917 | 0.561 |
DOC_USP7_MATH_1 | 258 | 262 | PF00917 | 0.611 |
DOC_USP7_MATH_1 | 28 | 32 | PF00917 | 0.481 |
DOC_USP7_MATH_1 | 79 | 83 | PF00917 | 0.560 |
DOC_USP7_UBL2_3 | 195 | 199 | PF12436 | 0.418 |
DOC_WW_Pin1_4 | 251 | 256 | PF00397 | 0.674 |
DOC_WW_Pin1_4 | 260 | 265 | PF00397 | 0.534 |
DOC_WW_Pin1_4 | 385 | 390 | PF00397 | 0.519 |
DOC_WW_Pin1_4 | 406 | 411 | PF00397 | 0.438 |
DOC_WW_Pin1_4 | 43 | 48 | PF00397 | 0.447 |
DOC_WW_Pin1_4 | 448 | 453 | PF00397 | 0.610 |
DOC_WW_Pin1_4 | 96 | 101 | PF00397 | 0.483 |
LIG_14-3-3_CanoR_1 | 116 | 121 | PF00244 | 0.572 |
LIG_14-3-3_CanoR_1 | 247 | 255 | PF00244 | 0.638 |
LIG_14-3-3_CanoR_1 | 303 | 312 | PF00244 | 0.544 |
LIG_14-3-3_CanoR_1 | 315 | 323 | PF00244 | 0.486 |
LIG_14-3-3_CanoR_1 | 343 | 349 | PF00244 | 0.436 |
LIG_14-3-3_CanoR_1 | 403 | 407 | PF00244 | 0.555 |
LIG_Actin_WH2_2 | 150 | 168 | PF00022 | 0.397 |
LIG_BRCT_BRCA1_1 | 308 | 312 | PF00533 | 0.483 |
LIG_DLG_GKlike_1 | 116 | 123 | PF00625 | 0.316 |
LIG_FHA_1 | 202 | 208 | PF00498 | 0.628 |
LIG_FHA_1 | 31 | 37 | PF00498 | 0.456 |
LIG_FHA_1 | 345 | 351 | PF00498 | 0.362 |
LIG_FHA_1 | 395 | 401 | PF00498 | 0.475 |
LIG_FHA_1 | 421 | 427 | PF00498 | 0.575 |
LIG_FHA_1 | 472 | 478 | PF00498 | 0.559 |
LIG_FHA_2 | 101 | 107 | PF00498 | 0.619 |
LIG_FHA_2 | 195 | 201 | PF00498 | 0.606 |
LIG_FHA_2 | 319 | 325 | PF00498 | 0.476 |
LIG_FHA_2 | 330 | 336 | PF00498 | 0.513 |
LIG_Integrin_isoDGR_2 | 463 | 465 | PF01839 | 0.620 |
LIG_LIR_Apic_2 | 438 | 444 | PF02991 | 0.495 |
LIG_LIR_Apic_2 | 448 | 452 | PF02991 | 0.523 |
LIG_LIR_Apic_2 | 95 | 100 | PF02991 | 0.471 |
LIG_LIR_Gen_1 | 128 | 139 | PF02991 | 0.413 |
LIG_LRP6_Inhibitor_1 | 477 | 483 | PF00058 | 0.512 |
LIG_MYND_1 | 385 | 389 | PF01753 | 0.396 |
LIG_NBox_RRM_1 | 313 | 323 | PF00076 | 0.392 |
LIG_NRBOX | 296 | 302 | PF00104 | 0.268 |
LIG_PCNA_yPIPBox_3 | 214 | 223 | PF02747 | 0.435 |
LIG_REV1ctd_RIR_1 | 310 | 319 | PF16727 | 0.388 |
LIG_SH2_CRK | 169 | 173 | PF00017 | 0.455 |
LIG_SH2_NCK_1 | 202 | 206 | PF00017 | 0.504 |
LIG_SH2_SRC | 333 | 336 | PF00017 | 0.487 |
LIG_SH2_STAP1 | 333 | 337 | PF00017 | 0.482 |
LIG_SH2_STAP1 | 37 | 41 | PF00017 | 0.284 |
LIG_SH2_STAP1 | 424 | 428 | PF00017 | 0.540 |
LIG_SH2_STAT5 | 349 | 352 | PF00017 | 0.266 |
LIG_SH2_STAT5 | 363 | 366 | PF00017 | 0.540 |
LIG_SH2_STAT5 | 481 | 484 | PF00017 | 0.492 |
LIG_SH2_STAT5 | 9 | 12 | PF00017 | 0.426 |
LIG_SH3_3 | 324 | 330 | PF00018 | 0.552 |
LIG_SH3_CIN85_PxpxPR_1 | 452 | 457 | PF14604 | 0.681 |
LIG_SUMO_SIM_anti_2 | 281 | 287 | PF11976 | 0.404 |
LIG_SUMO_SIM_anti_2 | 370 | 375 | PF11976 | 0.468 |
LIG_TRAF2_1 | 208 | 211 | PF00917 | 0.687 |
LIG_TRAF2_1 | 332 | 335 | PF00917 | 0.505 |
LIG_TYR_ITIM | 157 | 162 | PF00017 | 0.409 |
LIG_UBA3_1 | 89 | 98 | PF00899 | 0.369 |
LIG_WW_3 | 465 | 469 | PF00397 | 0.545 |
MOD_CDK_SPK_2 | 452 | 457 | PF00069 | 0.649 |
MOD_CDK_SPxxK_3 | 406 | 413 | PF00069 | 0.443 |
MOD_CK1_1 | 109 | 115 | PF00069 | 0.645 |
MOD_CK1_1 | 118 | 124 | PF00069 | 0.483 |
MOD_CK1_1 | 190 | 196 | PF00069 | 0.680 |
MOD_CK1_1 | 29 | 35 | PF00069 | 0.468 |
MOD_CK1_1 | 308 | 314 | PF00069 | 0.435 |
MOD_CK1_1 | 380 | 386 | PF00069 | 0.353 |
MOD_CK1_1 | 409 | 415 | PF00069 | 0.721 |
MOD_CK2_1 | 116 | 122 | PF00069 | 0.534 |
MOD_CK2_1 | 178 | 184 | PF00069 | 0.412 |
MOD_CK2_1 | 194 | 200 | PF00069 | 0.497 |
MOD_CK2_1 | 318 | 324 | PF00069 | 0.497 |
MOD_CK2_1 | 329 | 335 | PF00069 | 0.520 |
MOD_CK2_1 | 59 | 65 | PF00069 | 0.511 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.682 |
MOD_GlcNHglycan | 122 | 126 | PF01048 | 0.489 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.449 |
MOD_GlcNHglycan | 16 | 19 | PF01048 | 0.665 |
MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.679 |
MOD_GlcNHglycan | 297 | 300 | PF01048 | 0.402 |
MOD_GlcNHglycan | 307 | 311 | PF01048 | 0.510 |
MOD_GlcNHglycan | 334 | 338 | PF01048 | 0.474 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.517 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.731 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.391 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.610 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.671 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.536 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.433 |
MOD_GSK3_1 | 329 | 336 | PF00069 | 0.646 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.448 |
MOD_GSK3_1 | 402 | 409 | PF00069 | 0.621 |
MOD_GSK3_1 | 448 | 455 | PF00069 | 0.670 |
MOD_GSK3_1 | 471 | 478 | PF00069 | 0.570 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.333 |
MOD_NEK2_1 | 115 | 120 | PF00069 | 0.557 |
MOD_NEK2_1 | 201 | 206 | PF00069 | 0.531 |
MOD_NEK2_1 | 234 | 239 | PF00069 | 0.362 |
MOD_NEK2_1 | 246 | 251 | PF00069 | 0.626 |
MOD_NEK2_1 | 26 | 31 | PF00069 | 0.523 |
MOD_NEK2_1 | 391 | 396 | PF00069 | 0.364 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.611 |
MOD_NEK2_2 | 111 | 116 | PF00069 | 0.358 |
MOD_NEK2_2 | 79 | 84 | PF00069 | 0.371 |
MOD_NEK2_2 | 92 | 97 | PF00069 | 0.259 |
MOD_PK_1 | 429 | 435 | PF00069 | 0.602 |
MOD_PKA_1 | 475 | 481 | PF00069 | 0.490 |
MOD_PKA_2 | 115 | 121 | PF00069 | 0.337 |
MOD_PKA_2 | 246 | 252 | PF00069 | 0.425 |
MOD_PKA_2 | 267 | 273 | PF00069 | 0.514 |
MOD_PKA_2 | 402 | 408 | PF00069 | 0.557 |
MOD_PKA_2 | 475 | 481 | PF00069 | 0.498 |
MOD_PKB_1 | 303 | 311 | PF00069 | 0.390 |
MOD_Plk_1 | 209 | 215 | PF00069 | 0.678 |
MOD_Plk_2-3 | 329 | 335 | PF00069 | 0.520 |
MOD_Plk_4 | 143 | 149 | PF00069 | 0.528 |
MOD_Plk_4 | 281 | 287 | PF00069 | 0.431 |
MOD_Plk_4 | 308 | 314 | PF00069 | 0.368 |
MOD_Plk_4 | 344 | 350 | PF00069 | 0.445 |
MOD_ProDKin_1 | 251 | 257 | PF00069 | 0.678 |
MOD_ProDKin_1 | 260 | 266 | PF00069 | 0.536 |
MOD_ProDKin_1 | 385 | 391 | PF00069 | 0.512 |
MOD_ProDKin_1 | 406 | 412 | PF00069 | 0.439 |
MOD_ProDKin_1 | 43 | 49 | PF00069 | 0.447 |
MOD_ProDKin_1 | 448 | 454 | PF00069 | 0.609 |
MOD_ProDKin_1 | 96 | 102 | PF00069 | 0.491 |
MOD_SUMO_rev_2 | 439 | 448 | PF00179 | 0.549 |
TRG_DiLeu_BaEn_2 | 271 | 277 | PF01217 | 0.417 |
TRG_DiLeu_BaEn_2 | 436 | 442 | PF01217 | 0.496 |
TRG_ENDOCYTIC_2 | 159 | 162 | PF00928 | 0.449 |
TRG_ENDOCYTIC_2 | 169 | 172 | PF00928 | 0.239 |
TRG_ER_diArg_1 | 231 | 233 | PF00400 | 0.427 |
TRG_ER_diArg_1 | 364 | 366 | PF00400 | 0.419 |
TRG_ER_diArg_1 | 374 | 376 | PF00400 | 0.316 |
TRG_ER_diArg_1 | 413 | 415 | PF00400 | 0.584 |
TRG_ER_diArg_1 | 467 | 469 | PF00400 | 0.598 |
TRG_ER_diArg_1 | 475 | 477 | PF00400 | 0.493 |
TRG_NLS_Bipartite_1 | 468 | 490 | PF00514 | 0.560 |
TRG_NLS_MonoCore_2 | 484 | 489 | PF00514 | 0.472 |
TRG_NLS_MonoExtN_4 | 483 | 490 | PF00514 | 0.475 |
TRG_Pf-PMV_PEXEL_1 | 232 | 236 | PF00026 | 0.425 |
TRG_Pf-PMV_PEXEL_1 | 375 | 379 | PF00026 | 0.430 |
TRG_Pf-PMV_PEXEL_1 | 440 | 445 | PF00026 | 0.404 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5S3 | Leptomonas seymouri | 58% | 100% |
A0A1X0P4N9 | Trypanosomatidae | 34% | 100% |
A0A3R7KSE1 | Trypanosoma rangeli | 33% | 100% |
A0A3S7X0E2 | Leishmania donovani | 80% | 100% |
A4I2L9 | Leishmania infantum | 80% | 100% |
D0A5N1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
E9AD09 | Leishmania major | 80% | 100% |
E9AYT4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
V5BSR3 | Trypanosoma cruzi | 32% | 100% |