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: A0A3S7WNM2
Term | Name | Level | Count |
---|---|---|---|
GO:0006417 | regulation of translation | 6 | 1 |
GO:0006448 | regulation of translational elongation | 7 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009058 | biosynthetic process | 2 | 1 |
GO:0009889 | regulation of biosynthetic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010468 | regulation of gene expression | 5 | 1 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 1 |
GO:0010608 | post-transcriptional regulation of gene expression | 6 | 1 |
GO:0017182 | peptidyl-diphthamide metabolic process | 7 | 1 |
GO:0017183 | peptidyl-diphthamide biosynthetic process from peptidyl-histidine | 4 | 1 |
GO:0018193 | peptidyl-amino acid modification | 5 | 1 |
GO:0018202 | peptidyl-histidine modification | 6 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 1 |
GO:0034248 | regulation of amide metabolic process | 5 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044249 | cellular biosynthetic process | 3 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051246 | regulation of protein metabolic process | 5 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:1900247 | regulation of cytoplasmic translational elongation | 8 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:2000112 | obsolete regulation of cellular macromolecule biosynthetic process | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
GO:0016787 | hydrolase activity | 2 | 1 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 1 |
GO:0052689 | carboxylic ester hydrolase activity | 4 | 1 |
GO:0061685 | diphthine methylesterase activity | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 106 | 110 | PF00656 | 0.762 |
CLV_C14_Caspase3-7 | 171 | 175 | PF00656 | 0.554 |
CLV_C14_Caspase3-7 | 282 | 286 | PF00656 | 0.753 |
CLV_C14_Caspase3-7 | 342 | 346 | PF00656 | 0.492 |
CLV_C14_Caspase3-7 | 510 | 514 | PF00656 | 0.483 |
CLV_C14_Caspase3-7 | 527 | 531 | PF00656 | 0.393 |
CLV_NRD_NRD_1 | 145 | 147 | PF00675 | 0.502 |
CLV_NRD_NRD_1 | 37 | 39 | PF00675 | 0.350 |
CLV_NRD_NRD_1 | 374 | 376 | PF00675 | 0.550 |
CLV_NRD_NRD_1 | 432 | 434 | PF00675 | 0.481 |
CLV_NRD_NRD_1 | 553 | 555 | PF00675 | 0.429 |
CLV_PCSK_KEX2_1 | 145 | 147 | PF00082 | 0.502 |
CLV_PCSK_KEX2_1 | 37 | 39 | PF00082 | 0.412 |
CLV_PCSK_KEX2_1 | 374 | 376 | PF00082 | 0.438 |
CLV_PCSK_KEX2_1 | 432 | 434 | PF00082 | 0.501 |
CLV_PCSK_KEX2_1 | 437 | 439 | PF00082 | 0.718 |
CLV_PCSK_KEX2_1 | 553 | 555 | PF00082 | 0.404 |
CLV_PCSK_PC1ET2_1 | 437 | 439 | PF00082 | 0.734 |
CLV_PCSK_PC7_1 | 428 | 434 | PF00082 | 0.441 |
CLV_PCSK_SKI1_1 | 241 | 245 | PF00082 | 0.450 |
CLV_PCSK_SKI1_1 | 392 | 396 | PF00082 | 0.513 |
CLV_PCSK_SKI1_1 | 80 | 84 | PF00082 | 0.556 |
DEG_APCC_DBOX_1 | 79 | 87 | PF00400 | 0.554 |
DEG_SCF_TRCP1_1 | 399 | 405 | PF00400 | 0.624 |
DEG_SPOP_SBC_1 | 94 | 98 | PF00917 | 0.560 |
DOC_CKS1_1 | 219 | 224 | PF01111 | 0.336 |
DOC_CKS1_1 | 42 | 47 | PF01111 | 0.426 |
DOC_CYCLIN_RxL_1 | 389 | 399 | PF00134 | 0.510 |
DOC_MAPK_gen_1 | 389 | 397 | PF00069 | 0.602 |
DOC_MAPK_gen_1 | 77 | 85 | PF00069 | 0.556 |
DOC_MAPK_MEF2A_6 | 27 | 36 | PF00069 | 0.504 |
DOC_MAPK_MEF2A_6 | 77 | 85 | PF00069 | 0.496 |
DOC_PP2B_LxvP_1 | 456 | 459 | PF13499 | 0.349 |
DOC_PP2B_LxvP_1 | 52 | 55 | PF13499 | 0.522 |
DOC_USP7_MATH_1 | 295 | 299 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 402 | 406 | PF00917 | 0.682 |
DOC_USP7_MATH_1 | 410 | 414 | PF00917 | 0.685 |
DOC_USP7_MATH_1 | 450 | 454 | PF00917 | 0.626 |
DOC_USP7_MATH_1 | 494 | 498 | PF00917 | 0.617 |
DOC_USP7_MATH_1 | 538 | 542 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 546 | 550 | PF00917 | 0.416 |
DOC_USP7_MATH_1 | 67 | 71 | PF00917 | 0.729 |
DOC_USP7_MATH_1 | 95 | 99 | PF00917 | 0.654 |
DOC_WW_Pin1_4 | 194 | 199 | PF00397 | 0.548 |
DOC_WW_Pin1_4 | 218 | 223 | PF00397 | 0.462 |
DOC_WW_Pin1_4 | 269 | 274 | PF00397 | 0.627 |
DOC_WW_Pin1_4 | 335 | 340 | PF00397 | 0.435 |
DOC_WW_Pin1_4 | 350 | 355 | PF00397 | 0.480 |
DOC_WW_Pin1_4 | 41 | 46 | PF00397 | 0.488 |
DOC_WW_Pin1_4 | 54 | 59 | PF00397 | 0.492 |
LIG_14-3-3_CanoR_1 | 145 | 153 | PF00244 | 0.551 |
LIG_14-3-3_CanoR_1 | 27 | 36 | PF00244 | 0.573 |
LIG_14-3-3_CanoR_1 | 296 | 303 | PF00244 | 0.519 |
LIG_14-3-3_CanoR_1 | 37 | 43 | PF00244 | 0.467 |
LIG_14-3-3_CanoR_1 | 432 | 439 | PF00244 | 0.600 |
LIG_14-3-3_CanoR_1 | 473 | 480 | PF00244 | 0.540 |
LIG_14-3-3_CanoR_1 | 93 | 102 | PF00244 | 0.498 |
LIG_Actin_WH2_2 | 79 | 95 | PF00022 | 0.476 |
LIG_AP2alpha_2 | 192 | 194 | PF02296 | 0.410 |
LIG_BIR_III_2 | 174 | 178 | PF00653 | 0.356 |
LIG_BRCT_BRCA1_1 | 160 | 164 | PF00533 | 0.506 |
LIG_eIF4E_1 | 219 | 225 | PF01652 | 0.327 |
LIG_FHA_1 | 145 | 151 | PF00498 | 0.546 |
LIG_FHA_1 | 164 | 170 | PF00498 | 0.407 |
LIG_FHA_1 | 219 | 225 | PF00498 | 0.535 |
LIG_FHA_1 | 228 | 234 | PF00498 | 0.328 |
LIG_FHA_1 | 242 | 248 | PF00498 | 0.419 |
LIG_FHA_1 | 255 | 261 | PF00498 | 0.475 |
LIG_FHA_1 | 297 | 303 | PF00498 | 0.553 |
LIG_FHA_1 | 336 | 342 | PF00498 | 0.455 |
LIG_FHA_1 | 351 | 357 | PF00498 | 0.350 |
LIG_FHA_1 | 450 | 456 | PF00498 | 0.521 |
LIG_FHA_1 | 8 | 14 | PF00498 | 0.546 |
LIG_FHA_2 | 4 | 10 | PF00498 | 0.598 |
LIG_FHA_2 | 508 | 514 | PF00498 | 0.551 |
LIG_FHA_2 | 534 | 540 | PF00498 | 0.669 |
LIG_LIR_Gen_1 | 308 | 317 | PF02991 | 0.487 |
LIG_LIR_Gen_1 | 353 | 361 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 308 | 314 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 353 | 358 | PF02991 | 0.372 |
LIG_MLH1_MIPbox_1 | 160 | 164 | PF16413 | 0.506 |
LIG_NRBOX | 343 | 349 | PF00104 | 0.379 |
LIG_NRBOX | 419 | 425 | PF00104 | 0.530 |
LIG_SH2_CRK | 311 | 315 | PF00017 | 0.485 |
LIG_SH2_NCK_1 | 125 | 129 | PF00017 | 0.447 |
LIG_SH2_NCK_1 | 236 | 240 | PF00017 | 0.456 |
LIG_SH2_SRC | 234 | 237 | PF00017 | 0.460 |
LIG_SH2_SRC | 361 | 364 | PF00017 | 0.387 |
LIG_SH2_STAP1 | 125 | 129 | PF00017 | 0.447 |
LIG_SH2_STAP1 | 361 | 365 | PF00017 | 0.337 |
LIG_SH2_STAP1 | 470 | 474 | PF00017 | 0.523 |
LIG_SH2_STAP1 | 518 | 522 | PF00017 | 0.361 |
LIG_SH2_STAP1 | 551 | 555 | PF00017 | 0.498 |
LIG_SH2_STAP1 | 90 | 94 | PF00017 | 0.465 |
LIG_SH2_STAT5 | 234 | 237 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 311 | 314 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 355 | 358 | PF00017 | 0.393 |
LIG_SH2_STAT5 | 489 | 492 | PF00017 | 0.418 |
LIG_SH3_2 | 270 | 275 | PF14604 | 0.444 |
LIG_SH3_3 | 154 | 160 | PF00018 | 0.448 |
LIG_SH3_3 | 17 | 23 | PF00018 | 0.506 |
LIG_SH3_3 | 187 | 193 | PF00018 | 0.511 |
LIG_SH3_3 | 196 | 202 | PF00018 | 0.526 |
LIG_SH3_3 | 264 | 270 | PF00018 | 0.583 |
LIG_SH3_3 | 39 | 45 | PF00018 | 0.506 |
LIG_SH3_3 | 519 | 525 | PF00018 | 0.471 |
LIG_SH3_3 | 52 | 58 | PF00018 | 0.516 |
LIG_SH3_3 | 75 | 81 | PF00018 | 0.710 |
LIG_SUMO_SIM_anti_2 | 362 | 369 | PF11976 | 0.451 |
LIG_SUMO_SIM_anti_2 | 452 | 459 | PF11976 | 0.501 |
LIG_SUMO_SIM_par_1 | 333 | 338 | PF11976 | 0.422 |
LIG_SUMO_SIM_par_1 | 366 | 372 | PF11976 | 0.505 |
LIG_TRAF2_1 | 475 | 478 | PF00917 | 0.496 |
LIG_TRFH_1 | 194 | 198 | PF08558 | 0.472 |
LIG_TYR_ITSM | 351 | 358 | PF00017 | 0.448 |
MOD_CDC14_SPxK_1 | 272 | 275 | PF00782 | 0.450 |
MOD_CDK_SPK_2 | 41 | 46 | PF00069 | 0.367 |
MOD_CDK_SPxK_1 | 269 | 275 | PF00069 | 0.446 |
MOD_CK1_1 | 11 | 17 | PF00069 | 0.624 |
MOD_CK1_1 | 158 | 164 | PF00069 | 0.502 |
MOD_CK1_1 | 165 | 171 | PF00069 | 0.593 |
MOD_CK1_1 | 227 | 233 | PF00069 | 0.470 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.422 |
MOD_CK1_1 | 444 | 450 | PF00069 | 0.519 |
MOD_CK1_1 | 57 | 63 | PF00069 | 0.560 |
MOD_CK1_1 | 66 | 72 | PF00069 | 0.718 |
MOD_CK1_1 | 97 | 103 | PF00069 | 0.573 |
MOD_CK2_1 | 234 | 240 | PF00069 | 0.501 |
MOD_CK2_1 | 3 | 9 | PF00069 | 0.631 |
MOD_CK2_1 | 357 | 363 | PF00069 | 0.350 |
MOD_CK2_1 | 472 | 478 | PF00069 | 0.496 |
MOD_CK2_1 | 494 | 500 | PF00069 | 0.594 |
MOD_CK2_1 | 546 | 552 | PF00069 | 0.472 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.572 |
MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.591 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.491 |
MOD_GlcNHglycan | 29 | 32 | PF01048 | 0.616 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.437 |
MOD_GlcNHglycan | 304 | 307 | PF01048 | 0.309 |
MOD_GlcNHglycan | 399 | 402 | PF01048 | 0.664 |
MOD_GlcNHglycan | 425 | 428 | PF01048 | 0.577 |
MOD_GlcNHglycan | 446 | 449 | PF01048 | 0.542 |
MOD_GlcNHglycan | 474 | 477 | PF01048 | 0.562 |
MOD_GlcNHglycan | 539 | 543 | PF01048 | 0.581 |
MOD_GlcNHglycan | 65 | 68 | PF01048 | 0.719 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.736 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.734 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.657 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.483 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.619 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.590 |
MOD_GSK3_1 | 357 | 364 | PF00069 | 0.363 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.741 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.579 |
MOD_N-GLC_1 | 418 | 423 | PF02516 | 0.531 |
MOD_N-GLC_1 | 450 | 455 | PF02516 | 0.562 |
MOD_NEK2_1 | 163 | 168 | PF00069 | 0.543 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.410 |
MOD_NEK2_1 | 224 | 229 | PF00069 | 0.449 |
MOD_NEK2_1 | 302 | 307 | PF00069 | 0.470 |
MOD_NEK2_1 | 397 | 402 | PF00069 | 0.616 |
MOD_NEK2_1 | 423 | 428 | PF00069 | 0.552 |
MOD_NEK2_2 | 546 | 551 | PF00069 | 0.471 |
MOD_OFUCOSY | 12 | 18 | PF10250 | 0.514 |
MOD_PIKK_1 | 241 | 247 | PF00454 | 0.468 |
MOD_PK_1 | 38 | 44 | PF00069 | 0.521 |
MOD_PKA_2 | 144 | 150 | PF00069 | 0.559 |
MOD_PKA_2 | 295 | 301 | PF00069 | 0.637 |
MOD_PKA_2 | 388 | 394 | PF00069 | 0.391 |
MOD_PKA_2 | 431 | 437 | PF00069 | 0.584 |
MOD_PKA_2 | 472 | 478 | PF00069 | 0.539 |
MOD_Plk_1 | 137 | 143 | PF00069 | 0.649 |
MOD_Plk_1 | 361 | 367 | PF00069 | 0.463 |
MOD_Plk_1 | 418 | 424 | PF00069 | 0.578 |
MOD_Plk_1 | 512 | 518 | PF00069 | 0.455 |
MOD_Plk_1 | 8 | 14 | PF00069 | 0.599 |
MOD_Plk_2-3 | 363 | 369 | PF00069 | 0.479 |
MOD_Plk_4 | 159 | 165 | PF00069 | 0.561 |
MOD_Plk_4 | 229 | 235 | PF00069 | 0.367 |
MOD_Plk_4 | 418 | 424 | PF00069 | 0.528 |
MOD_Plk_4 | 485 | 491 | PF00069 | 0.519 |
MOD_Plk_4 | 512 | 518 | PF00069 | 0.455 |
MOD_Plk_4 | 546 | 552 | PF00069 | 0.370 |
MOD_ProDKin_1 | 194 | 200 | PF00069 | 0.546 |
MOD_ProDKin_1 | 218 | 224 | PF00069 | 0.453 |
MOD_ProDKin_1 | 269 | 275 | PF00069 | 0.630 |
MOD_ProDKin_1 | 335 | 341 | PF00069 | 0.438 |
MOD_ProDKin_1 | 350 | 356 | PF00069 | 0.473 |
MOD_ProDKin_1 | 41 | 47 | PF00069 | 0.484 |
MOD_ProDKin_1 | 54 | 60 | PF00069 | 0.503 |
MOD_SUMO_rev_2 | 434 | 439 | PF00179 | 0.585 |
TRG_DiLeu_BaEn_1 | 363 | 368 | PF01217 | 0.368 |
TRG_ENDOCYTIC_2 | 125 | 128 | PF00928 | 0.479 |
TRG_ENDOCYTIC_2 | 311 | 314 | PF00928 | 0.486 |
TRG_ENDOCYTIC_2 | 355 | 358 | PF00928 | 0.365 |
TRG_ER_diArg_1 | 327 | 330 | PF00400 | 0.519 |
TRG_ER_diArg_1 | 36 | 38 | PF00400 | 0.376 |
TRG_ER_diArg_1 | 373 | 375 | PF00400 | 0.548 |
TRG_ER_diArg_1 | 553 | 555 | PF00400 | 0.436 |
TRG_Pf-PMV_PEXEL_1 | 204 | 209 | PF00026 | 0.507 |
TRG_PTS1 | 564 | 567 | PF00515 | 0.466 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IHU3 | Leptomonas seymouri | 50% | 100% |
A0A1X0NJL9 | Trypanosomatidae | 30% | 100% |
A0A3R7NH89 | Trypanosoma rangeli | 30% | 100% |
A4H3F3 | Leishmania braziliensis | 75% | 100% |
A4HRQ7 | Leishmania infantum | 99% | 100% |
C9ZJ47 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
E9ACD6 | Leishmania major | 90% | 100% |
E9AJM4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
V5BER3 | Trypanosoma cruzi | 29% | 100% |