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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4IA95
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0007165 | signal transduction | 2 | 1 |
GO:0007264 | small GTPase mediated signal transduction | 4 | 1 |
GO:0007265 | Ras protein signal transduction | 5 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016567 | protein ubiquitination | 7 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0032446 | protein modification by small protein conjugation | 6 | 1 |
GO:0035556 | intracellular signal transduction | 3 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 12 |
GO:0008270 | zinc ion binding | 6 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043169 | cation binding | 3 | 12 |
GO:0046872 | metal ion binding | 4 | 12 |
GO:0046914 | transition metal ion binding | 5 | 12 |
GO:0003824 | catalytic activity | 1 | 2 |
GO:0004842 | ubiquitin-protein transferase activity | 4 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0019787 | ubiquitin-like protein transferase activity | 3 | 1 |
GO:0061630 | ubiquitin protein ligase activity | 5 | 1 |
GO:0061659 | ubiquitin-like protein ligase activity | 4 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
GO:0016787 | hydrolase activity | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 115 | 119 | PF00656 | 0.289 |
CLV_C14_Caspase3-7 | 175 | 179 | PF00656 | 0.515 |
CLV_C14_Caspase3-7 | 395 | 399 | PF00656 | 0.531 |
CLV_C14_Caspase3-7 | 75 | 79 | PF00656 | 0.634 |
CLV_NRD_NRD_1 | 235 | 237 | PF00675 | 0.489 |
CLV_NRD_NRD_1 | 36 | 38 | PF00675 | 0.307 |
CLV_NRD_NRD_1 | 465 | 467 | PF00675 | 0.604 |
CLV_NRD_NRD_1 | 539 | 541 | PF00675 | 0.562 |
CLV_NRD_NRD_1 | 574 | 576 | PF00675 | 0.719 |
CLV_PCSK_KEX2_1 | 235 | 237 | PF00082 | 0.489 |
CLV_PCSK_KEX2_1 | 400 | 402 | PF00082 | 0.471 |
CLV_PCSK_KEX2_1 | 464 | 466 | PF00082 | 0.574 |
CLV_PCSK_KEX2_1 | 539 | 541 | PF00082 | 0.594 |
CLV_PCSK_KEX2_1 | 574 | 576 | PF00082 | 0.725 |
CLV_PCSK_PC1ET2_1 | 400 | 402 | PF00082 | 0.514 |
CLV_PCSK_PC1ET2_1 | 464 | 466 | PF00082 | 0.606 |
CLV_PCSK_SKI1_1 | 38 | 42 | PF00082 | 0.331 |
CLV_PCSK_SKI1_1 | 380 | 384 | PF00082 | 0.597 |
CLV_PCSK_SKI1_1 | 400 | 404 | PF00082 | 0.247 |
CLV_PCSK_SKI1_1 | 476 | 480 | PF00082 | 0.564 |
CLV_PCSK_SKI1_1 | 500 | 504 | PF00082 | 0.530 |
CLV_PCSK_SKI1_1 | 522 | 526 | PF00082 | 0.568 |
CLV_PCSK_SKI1_1 | 552 | 556 | PF00082 | 0.696 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.293 |
DEG_SPOP_SBC_1 | 157 | 161 | PF00917 | 0.449 |
DEG_SPOP_SBC_1 | 72 | 76 | PF00917 | 0.611 |
DOC_CKS1_1 | 45 | 50 | PF01111 | 0.511 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 476 | 482 | PF00134 | 0.550 |
DOC_MAPK_gen_1 | 8 | 17 | PF00069 | 0.491 |
DOC_MAPK_MEF2A_6 | 266 | 274 | PF00069 | 0.513 |
DOC_PP4_FxxP_1 | 45 | 48 | PF00568 | 0.378 |
DOC_USP7_MATH_1 | 120 | 124 | PF00917 | 0.445 |
DOC_USP7_MATH_1 | 133 | 137 | PF00917 | 0.450 |
DOC_USP7_MATH_1 | 253 | 257 | PF00917 | 0.513 |
DOC_USP7_MATH_1 | 350 | 354 | PF00917 | 0.698 |
DOC_USP7_MATH_1 | 453 | 457 | PF00917 | 0.611 |
DOC_USP7_MATH_1 | 48 | 52 | PF00917 | 0.451 |
DOC_USP7_MATH_1 | 502 | 506 | PF00917 | 0.575 |
DOC_USP7_MATH_1 | 72 | 76 | PF00917 | 0.670 |
DOC_USP7_MATH_1 | 79 | 83 | PF00917 | 0.700 |
DOC_USP7_MATH_1 | 89 | 93 | PF00917 | 0.327 |
DOC_USP7_UBL2_3 | 368 | 372 | PF12436 | 0.558 |
DOC_USP7_UBL2_3 | 377 | 381 | PF12436 | 0.459 |
DOC_USP7_UBL2_3 | 38 | 42 | PF12436 | 0.341 |
DOC_WW_Pin1_4 | 206 | 211 | PF00397 | 0.484 |
DOC_WW_Pin1_4 | 360 | 365 | PF00397 | 0.706 |
DOC_WW_Pin1_4 | 44 | 49 | PF00397 | 0.512 |
LIG_14-3-3_CanoR_1 | 158 | 163 | PF00244 | 0.459 |
LIG_14-3-3_CanoR_1 | 429 | 439 | PF00244 | 0.670 |
LIG_14-3-3_CanoR_1 | 465 | 475 | PF00244 | 0.525 |
LIG_14-3-3_CanoR_1 | 516 | 524 | PF00244 | 0.474 |
LIG_Actin_WH2_2 | 489 | 506 | PF00022 | 0.500 |
LIG_AP2alpha_2 | 269 | 271 | PF02296 | 0.464 |
LIG_EH1_1 | 318 | 326 | PF00400 | 0.567 |
LIG_FHA_1 | 10 | 16 | PF00498 | 0.402 |
LIG_FHA_1 | 222 | 228 | PF00498 | 0.497 |
LIG_FHA_1 | 304 | 310 | PF00498 | 0.451 |
LIG_FHA_1 | 45 | 51 | PF00498 | 0.383 |
LIG_FHA_1 | 466 | 472 | PF00498 | 0.620 |
LIG_FHA_1 | 487 | 493 | PF00498 | 0.541 |
LIG_FHA_1 | 91 | 97 | PF00498 | 0.495 |
LIG_FHA_2 | 17 | 23 | PF00498 | 0.503 |
LIG_FHA_2 | 173 | 179 | PF00498 | 0.538 |
LIG_FHA_2 | 432 | 438 | PF00498 | 0.612 |
LIG_FHA_2 | 447 | 453 | PF00498 | 0.589 |
LIG_FHA_2 | 482 | 488 | PF00498 | 0.579 |
LIG_FHA_2 | 525 | 531 | PF00498 | 0.446 |
LIG_LIR_Apic_2 | 183 | 189 | PF02991 | 0.380 |
LIG_LIR_Apic_2 | 44 | 48 | PF02991 | 0.392 |
LIG_LIR_Gen_1 | 269 | 279 | PF02991 | 0.453 |
LIG_LIR_Gen_1 | 282 | 289 | PF02991 | 0.454 |
LIG_LIR_Gen_1 | 331 | 338 | PF02991 | 0.604 |
LIG_LIR_Gen_1 | 443 | 451 | PF02991 | 0.623 |
LIG_LIR_Gen_1 | 51 | 60 | PF02991 | 0.425 |
LIG_LIR_Nem_3 | 183 | 188 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 269 | 274 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 331 | 337 | PF02991 | 0.598 |
LIG_LIR_Nem_3 | 44 | 49 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 443 | 447 | PF02991 | 0.614 |
LIG_LIR_Nem_3 | 449 | 454 | PF02991 | 0.569 |
LIG_LIR_Nem_3 | 51 | 57 | PF02991 | 0.290 |
LIG_PCNA_PIPBox_1 | 99 | 108 | PF02747 | 0.425 |
LIG_Pex14_2 | 41 | 45 | PF04695 | 0.349 |
LIG_SH2_CRK | 389 | 393 | PF00017 | 0.569 |
LIG_SH2_PTP2 | 444 | 447 | PF00017 | 0.453 |
LIG_SH2_PTP2 | 54 | 57 | PF00017 | 0.267 |
LIG_SH2_STAP1 | 378 | 382 | PF00017 | 0.520 |
LIG_SH2_STAP1 | 389 | 393 | PF00017 | 0.413 |
LIG_SH2_STAP1 | 404 | 408 | PF00017 | 0.457 |
LIG_SH2_STAT3 | 205 | 208 | PF00017 | 0.529 |
LIG_SH2_STAT3 | 243 | 246 | PF00017 | 0.509 |
LIG_SH2_STAT3 | 404 | 407 | PF00017 | 0.572 |
LIG_SH2_STAT5 | 163 | 166 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 187 | 190 | PF00017 | 0.351 |
LIG_SH2_STAT5 | 278 | 281 | PF00017 | 0.492 |
LIG_SH2_STAT5 | 444 | 447 | PF00017 | 0.561 |
LIG_SH2_STAT5 | 54 | 57 | PF00017 | 0.267 |
LIG_SH3_1 | 186 | 192 | PF00018 | 0.446 |
LIG_SH3_3 | 186 | 192 | PF00018 | 0.446 |
LIG_SUMO_SIM_anti_2 | 139 | 145 | PF11976 | 0.467 |
LIG_SUMO_SIM_anti_2 | 551 | 557 | PF11976 | 0.613 |
LIG_SUMO_SIM_par_1 | 12 | 23 | PF11976 | 0.452 |
LIG_SUMO_SIM_par_1 | 320 | 329 | PF11976 | 0.446 |
LIG_SUMO_SIM_par_1 | 92 | 97 | PF11976 | 0.327 |
LIG_TYR_ITIM | 2 | 7 | PF00017 | 0.306 |
LIG_TYR_ITSM | 181 | 188 | PF00017 | 0.399 |
LIG_UBA3_1 | 458 | 464 | PF00899 | 0.514 |
MOD_CK1_1 | 100 | 106 | PF00069 | 0.376 |
MOD_CK1_1 | 20 | 26 | PF00069 | 0.483 |
MOD_CK1_1 | 221 | 227 | PF00069 | 0.546 |
MOD_CK1_1 | 328 | 334 | PF00069 | 0.471 |
MOD_CK1_1 | 44 | 50 | PF00069 | 0.388 |
MOD_CK1_1 | 498 | 504 | PF00069 | 0.554 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.467 |
MOD_CK2_1 | 16 | 22 | PF00069 | 0.523 |
MOD_CK2_1 | 431 | 437 | PF00069 | 0.591 |
MOD_CK2_1 | 446 | 452 | PF00069 | 0.592 |
MOD_CK2_1 | 481 | 487 | PF00069 | 0.547 |
MOD_CK2_1 | 517 | 523 | PF00069 | 0.496 |
MOD_Cter_Amidation | 572 | 575 | PF01082 | 0.656 |
MOD_GlcNHglycan | 102 | 105 | PF01048 | 0.469 |
MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.343 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.429 |
MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.513 |
MOD_GlcNHglycan | 255 | 258 | PF01048 | 0.619 |
MOD_GlcNHglycan | 352 | 355 | PF01048 | 0.667 |
MOD_GlcNHglycan | 374 | 377 | PF01048 | 0.647 |
MOD_GlcNHglycan | 413 | 416 | PF01048 | 0.682 |
MOD_GlcNHglycan | 558 | 561 | PF01048 | 0.664 |
MOD_GlcNHglycan | 81 | 84 | PF01048 | 0.676 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.360 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.438 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.419 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.531 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.508 |
MOD_GSK3_1 | 498 | 505 | PF00069 | 0.457 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.650 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.454 |
MOD_NEK2_1 | 198 | 203 | PF00069 | 0.469 |
MOD_NEK2_1 | 226 | 231 | PF00069 | 0.450 |
MOD_NEK2_1 | 324 | 329 | PF00069 | 0.506 |
MOD_NEK2_1 | 382 | 387 | PF00069 | 0.569 |
MOD_NEK2_1 | 403 | 408 | PF00069 | 0.542 |
MOD_NEK2_1 | 41 | 46 | PF00069 | 0.360 |
MOD_NEK2_1 | 515 | 520 | PF00069 | 0.479 |
MOD_NEK2_1 | 524 | 529 | PF00069 | 0.396 |
MOD_NEK2_1 | 77 | 82 | PF00069 | 0.718 |
MOD_OFUCOSY | 225 | 231 | PF10250 | 0.374 |
MOD_PIKK_1 | 204 | 210 | PF00454 | 0.555 |
MOD_PIKK_1 | 218 | 224 | PF00454 | 0.345 |
MOD_PIKK_1 | 303 | 309 | PF00454 | 0.455 |
MOD_PIKK_1 | 403 | 409 | PF00454 | 0.579 |
MOD_PIKK_1 | 534 | 540 | PF00454 | 0.574 |
MOD_PIKK_1 | 9 | 15 | PF00454 | 0.453 |
MOD_PKA_1 | 380 | 386 | PF00069 | 0.619 |
MOD_PKA_1 | 465 | 471 | PF00069 | 0.592 |
MOD_PKA_2 | 157 | 163 | PF00069 | 0.486 |
MOD_PKA_2 | 465 | 471 | PF00069 | 0.539 |
MOD_PKA_2 | 515 | 521 | PF00069 | 0.497 |
MOD_PKA_2 | 573 | 579 | PF00069 | 0.770 |
MOD_PKA_2 | 9 | 15 | PF00069 | 0.428 |
MOD_Plk_1 | 198 | 204 | PF00069 | 0.481 |
MOD_Plk_1 | 487 | 493 | PF00069 | 0.504 |
MOD_Plk_1 | 87 | 93 | PF00069 | 0.426 |
MOD_Plk_4 | 139 | 145 | PF00069 | 0.438 |
MOD_Plk_4 | 158 | 164 | PF00069 | 0.490 |
MOD_Plk_4 | 181 | 187 | PF00069 | 0.500 |
MOD_Plk_4 | 24 | 30 | PF00069 | 0.310 |
MOD_Plk_4 | 330 | 336 | PF00069 | 0.589 |
MOD_Plk_4 | 41 | 47 | PF00069 | 0.268 |
MOD_Plk_4 | 453 | 459 | PF00069 | 0.552 |
MOD_ProDKin_1 | 206 | 212 | PF00069 | 0.476 |
MOD_ProDKin_1 | 360 | 366 | PF00069 | 0.700 |
MOD_ProDKin_1 | 44 | 50 | PF00069 | 0.508 |
MOD_SUMO_for_1 | 259 | 262 | PF00179 | 0.508 |
MOD_SUMO_for_1 | 393 | 396 | PF00179 | 0.532 |
MOD_SUMO_for_1 | 478 | 481 | PF00179 | 0.520 |
MOD_SUMO_rev_2 | 365 | 374 | PF00179 | 0.642 |
MOD_SUMO_rev_2 | 375 | 383 | PF00179 | 0.556 |
MOD_SUMO_rev_2 | 395 | 402 | PF00179 | 0.535 |
MOD_SUMO_rev_2 | 518 | 527 | PF00179 | 0.521 |
TRG_DiLeu_BaEn_4 | 487 | 493 | PF01217 | 0.587 |
TRG_DiLeu_BaLyEn_6 | 31 | 36 | PF01217 | 0.402 |
TRG_ENDOCYTIC_2 | 185 | 188 | PF00928 | 0.340 |
TRG_ENDOCYTIC_2 | 284 | 287 | PF00928 | 0.513 |
TRG_ENDOCYTIC_2 | 389 | 392 | PF00928 | 0.563 |
TRG_ENDOCYTIC_2 | 4 | 7 | PF00928 | 0.303 |
TRG_ENDOCYTIC_2 | 444 | 447 | PF00928 | 0.601 |
TRG_ENDOCYTIC_2 | 54 | 57 | PF00928 | 0.286 |
TRG_ER_diArg_1 | 235 | 237 | PF00400 | 0.489 |
TRG_ER_diArg_1 | 539 | 541 | PF00400 | 0.565 |
TRG_NLS_MonoExtN_4 | 34 | 41 | PF00514 | 0.311 |
TRG_Pf-PMV_PEXEL_1 | 401 | 405 | PF00026 | 0.556 |
TRG_Pf-PMV_PEXEL_1 | 522 | 526 | PF00026 | 0.536 |
TRG_Pf-PMV_PEXEL_1 | 539 | 544 | PF00026 | 0.461 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAV0 | Leptomonas seymouri | 63% | 98% |
A0A0S4ILW6 | Bodo saltans | 28% | 100% |
A0A1X0PAX0 | Trypanosomatidae | 33% | 100% |
A0A3Q8IEL0 | Leishmania donovani | 100% | 100% |
A0A422NNH1 | Trypanosoma rangeli | 33% | 100% |
A4HB46 | Leishmania braziliensis | 83% | 100% |
C9ZLZ9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
E9B5B7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
Q4Q2L6 | Leishmania major | 92% | 99% |
Q99MP8 | Mus musculus | 23% | 99% |
V5DLZ1 | Trypanosoma cruzi | 34% | 100% |