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 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4QC65
Term | Name | Level | Count |
---|---|---|---|
GO:0008152 | metabolic process | 1 | 2 |
GO:0032259 | methylation | 2 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 11 |
GO:0003747 | translation release factor activity | 5 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0008079 | translation termination factor activity | 4 | 11 |
GO:0008135 | translation factor activity, RNA binding | 3 | 11 |
GO:0045182 | translation regulator activity | 1 | 11 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
GO:0003824 | catalytic activity | 1 | 2 |
GO:0008168 | methyltransferase activity | 4 | 2 |
GO:0016740 | transferase activity | 2 | 2 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 191 | 195 | PF00656 | 0.504 |
CLV_C14_Caspase3-7 | 418 | 422 | PF00656 | 0.411 |
CLV_C14_Caspase3-7 | 490 | 494 | PF00656 | 0.442 |
CLV_NRD_NRD_1 | 117 | 119 | PF00675 | 0.624 |
CLV_NRD_NRD_1 | 138 | 140 | PF00675 | 0.576 |
CLV_NRD_NRD_1 | 249 | 251 | PF00675 | 0.453 |
CLV_NRD_NRD_1 | 257 | 259 | PF00675 | 0.442 |
CLV_NRD_NRD_1 | 338 | 340 | PF00675 | 0.356 |
CLV_NRD_NRD_1 | 412 | 414 | PF00675 | 0.430 |
CLV_NRD_NRD_1 | 512 | 514 | PF00675 | 0.257 |
CLV_NRD_NRD_1 | 88 | 90 | PF00675 | 0.696 |
CLV_PCSK_FUR_1 | 254 | 258 | PF00082 | 0.467 |
CLV_PCSK_KEX2_1 | 101 | 103 | PF00082 | 0.676 |
CLV_PCSK_KEX2_1 | 256 | 258 | PF00082 | 0.464 |
CLV_PCSK_KEX2_1 | 313 | 315 | PF00082 | 0.482 |
CLV_PCSK_KEX2_1 | 338 | 340 | PF00082 | 0.356 |
CLV_PCSK_KEX2_1 | 412 | 414 | PF00082 | 0.430 |
CLV_PCSK_KEX2_1 | 449 | 451 | PF00082 | 0.471 |
CLV_PCSK_KEX2_1 | 512 | 514 | PF00082 | 0.257 |
CLV_PCSK_KEX2_1 | 88 | 90 | PF00082 | 0.683 |
CLV_PCSK_PC1ET2_1 | 101 | 103 | PF00082 | 0.570 |
CLV_PCSK_PC1ET2_1 | 313 | 315 | PF00082 | 0.348 |
CLV_PCSK_PC1ET2_1 | 449 | 451 | PF00082 | 0.471 |
CLV_PCSK_SKI1_1 | 174 | 178 | PF00082 | 0.589 |
CLV_PCSK_SKI1_1 | 200 | 204 | PF00082 | 0.542 |
CLV_PCSK_SKI1_1 | 207 | 211 | PF00082 | 0.537 |
CLV_PCSK_SKI1_1 | 446 | 450 | PF00082 | 0.571 |
CLV_PCSK_SKI1_1 | 495 | 499 | PF00082 | 0.254 |
CLV_PCSK_SKI1_1 | 89 | 93 | PF00082 | 0.652 |
DEG_APCC_DBOX_1 | 171 | 179 | PF00400 | 0.418 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.518 |
DEG_SPOP_SBC_1 | 226 | 230 | PF00917 | 0.531 |
DEG_SPOP_SBC_1 | 37 | 41 | PF00917 | 0.365 |
DOC_ANK_TNKS_1 | 458 | 465 | PF00023 | 0.431 |
DOC_CYCLIN_RxL_1 | 507 | 519 | PF00134 | 0.446 |
DOC_MAPK_gen_1 | 174 | 184 | PF00069 | 0.436 |
DOC_MAPK_gen_1 | 254 | 264 | PF00069 | 0.429 |
DOC_MAPK_MEF2A_6 | 256 | 264 | PF00069 | 0.424 |
DOC_MAPK_RevD_3 | 124 | 140 | PF00069 | 0.501 |
DOC_PP1_RVXF_1 | 510 | 517 | PF00149 | 0.446 |
DOC_USP7_MATH_1 | 220 | 224 | PF00917 | 0.574 |
DOC_USP7_MATH_1 | 244 | 248 | PF00917 | 0.525 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.365 |
DOC_USP7_MATH_1 | 394 | 398 | PF00917 | 0.504 |
DOC_USP7_MATH_1 | 417 | 421 | PF00917 | 0.481 |
DOC_USP7_MATH_1 | 438 | 442 | PF00917 | 0.346 |
DOC_USP7_MATH_1 | 458 | 462 | PF00917 | 0.397 |
DOC_USP7_MATH_1 | 491 | 495 | PF00917 | 0.442 |
DOC_USP7_MATH_1 | 72 | 76 | PF00917 | 0.702 |
DOC_USP7_MATH_1 | 79 | 83 | PF00917 | 0.634 |
DOC_USP7_UBL2_3 | 25 | 29 | PF12436 | 0.483 |
DOC_WW_Pin1_4 | 423 | 428 | PF00397 | 0.668 |
DOC_WW_Pin1_4 | 83 | 88 | PF00397 | 0.700 |
LIG_14-3-3_CanoR_1 | 200 | 209 | PF00244 | 0.558 |
LIG_14-3-3_CanoR_1 | 383 | 393 | PF00244 | 0.576 |
LIG_14-3-3_CanoR_1 | 450 | 454 | PF00244 | 0.430 |
LIG_Actin_WH2_2 | 178 | 195 | PF00022 | 0.488 |
LIG_BIR_III_2 | 391 | 395 | PF00653 | 0.517 |
LIG_BRCT_BRCA1_1 | 363 | 367 | PF00533 | 0.415 |
LIG_BRCT_BRCA1_1 | 368 | 372 | PF00533 | 0.463 |
LIG_CaM_IQ_9 | 154 | 169 | PF13499 | 0.430 |
LIG_FHA_1 | 227 | 233 | PF00498 | 0.593 |
LIG_FHA_1 | 39 | 45 | PF00498 | 0.628 |
LIG_FHA_1 | 556 | 562 | PF00498 | 0.530 |
LIG_LIR_Gen_1 | 127 | 136 | PF02991 | 0.405 |
LIG_LIR_Gen_1 | 228 | 238 | PF02991 | 0.493 |
LIG_LIR_Gen_1 | 301 | 311 | PF02991 | 0.419 |
LIG_LIR_Gen_1 | 348 | 356 | PF02991 | 0.374 |
LIG_LIR_Gen_1 | 364 | 374 | PF02991 | 0.210 |
LIG_LIR_Gen_1 | 473 | 484 | PF02991 | 0.535 |
LIG_LIR_Nem_3 | 127 | 133 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 145 | 150 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 228 | 234 | PF02991 | 0.580 |
LIG_LIR_Nem_3 | 301 | 307 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 348 | 353 | PF02991 | 0.372 |
LIG_LIR_Nem_3 | 364 | 370 | PF02991 | 0.208 |
LIG_LIR_Nem_3 | 473 | 479 | PF02991 | 0.535 |
LIG_MLH1_MIPbox_1 | 363 | 367 | PF16413 | 0.246 |
LIG_NRBOX | 233 | 239 | PF00104 | 0.462 |
LIG_Pex14_2 | 402 | 406 | PF04695 | 0.311 |
LIG_SH2_CRK | 350 | 354 | PF00017 | 0.385 |
LIG_SH2_CRK | 476 | 480 | PF00017 | 0.548 |
LIG_SH2_PTP2 | 231 | 234 | PF00017 | 0.422 |
LIG_SH2_PTP2 | 333 | 336 | PF00017 | 0.477 |
LIG_SH2_STAP1 | 350 | 354 | PF00017 | 0.378 |
LIG_SH2_STAP1 | 404 | 408 | PF00017 | 0.393 |
LIG_SH2_STAP1 | 487 | 491 | PF00017 | 0.510 |
LIG_SH2_STAT3 | 148 | 151 | PF00017 | 0.419 |
LIG_SH2_STAT5 | 231 | 234 | PF00017 | 0.537 |
LIG_SH2_STAT5 | 333 | 336 | PF00017 | 0.416 |
LIG_SH2_STAT5 | 340 | 343 | PF00017 | 0.360 |
LIG_SH2_STAT5 | 366 | 369 | PF00017 | 0.518 |
LIG_SH2_STAT5 | 487 | 490 | PF00017 | 0.445 |
LIG_SUMO_SIM_anti_2 | 181 | 188 | PF11976 | 0.419 |
LIG_SUMO_SIM_anti_2 | 566 | 571 | PF11976 | 0.507 |
LIG_SxIP_EBH_1 | 23 | 35 | PF03271 | 0.478 |
LIG_TRAF2_1 | 295 | 298 | PF00917 | 0.601 |
LIG_TRAF2_1 | 521 | 524 | PF00917 | 0.498 |
LIG_UBA3_1 | 26 | 35 | PF00899 | 0.658 |
LIG_WRC_WIRS_1 | 353 | 358 | PF05994 | 0.437 |
MOD_CDC14_SPxK_1 | 86 | 89 | PF00782 | 0.502 |
MOD_CDK_SPK_2 | 83 | 88 | PF00069 | 0.550 |
MOD_CDK_SPxK_1 | 83 | 89 | PF00069 | 0.507 |
MOD_CK1_1 | 106 | 112 | PF00069 | 0.596 |
MOD_CK1_1 | 170 | 176 | PF00069 | 0.424 |
MOD_CK1_1 | 195 | 201 | PF00069 | 0.483 |
MOD_CK1_1 | 269 | 275 | PF00069 | 0.515 |
MOD_CK1_1 | 496 | 502 | PF00069 | 0.495 |
MOD_CK1_1 | 58 | 64 | PF00069 | 0.717 |
MOD_CK1_1 | 73 | 79 | PF00069 | 0.697 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.657 |
MOD_CK2_1 | 110 | 116 | PF00069 | 0.541 |
MOD_CK2_1 | 149 | 155 | PF00069 | 0.468 |
MOD_CK2_1 | 496 | 502 | PF00069 | 0.507 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.579 |
MOD_GlcNHglycan | 396 | 399 | PF01048 | 0.441 |
MOD_GlcNHglycan | 434 | 437 | PF01048 | 0.456 |
MOD_GlcNHglycan | 440 | 443 | PF01048 | 0.419 |
MOD_GlcNHglycan | 460 | 463 | PF01048 | 0.182 |
MOD_GlcNHglycan | 495 | 498 | PF01048 | 0.231 |
MOD_GlcNHglycan | 65 | 68 | PF01048 | 0.589 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.602 |
MOD_GlcNHglycan | 81 | 84 | PF01048 | 0.555 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.573 |
MOD_GSK3_1 | 163 | 170 | PF00069 | 0.556 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.609 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.412 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.478 |
MOD_GSK3_1 | 361 | 368 | PF00069 | 0.397 |
MOD_GSK3_1 | 454 | 461 | PF00069 | 0.492 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.642 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.556 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.579 |
MOD_N-GLC_1 | 103 | 108 | PF02516 | 0.731 |
MOD_N-GLC_1 | 269 | 274 | PF02516 | 0.474 |
MOD_N-GLC_1 | 468 | 473 | PF02516 | 0.227 |
MOD_N-GLC_1 | 516 | 521 | PF02516 | 0.278 |
MOD_NEK2_1 | 103 | 108 | PF00069 | 0.697 |
MOD_NEK2_1 | 192 | 197 | PF00069 | 0.571 |
MOD_NEK2_1 | 202 | 207 | PF00069 | 0.430 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.437 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.546 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.502 |
MOD_NEK2_1 | 406 | 411 | PF00069 | 0.376 |
MOD_NEK2_1 | 431 | 436 | PF00069 | 0.339 |
MOD_NEK2_1 | 516 | 521 | PF00069 | 0.512 |
MOD_NEK2_1 | 60 | 65 | PF00069 | 0.694 |
MOD_PIKK_1 | 200 | 206 | PF00454 | 0.650 |
MOD_PIKK_1 | 293 | 299 | PF00454 | 0.500 |
MOD_PIKK_1 | 4 | 10 | PF00454 | 0.525 |
MOD_PIKK_1 | 470 | 476 | PF00454 | 0.451 |
MOD_PK_1 | 449 | 455 | PF00069 | 0.480 |
MOD_PKA_1 | 449 | 455 | PF00069 | 0.477 |
MOD_PKA_2 | 192 | 198 | PF00069 | 0.500 |
MOD_PKA_2 | 449 | 455 | PF00069 | 0.446 |
MOD_PKA_2 | 458 | 464 | PF00069 | 0.443 |
MOD_Plk_1 | 167 | 173 | PF00069 | 0.445 |
MOD_Plk_1 | 269 | 275 | PF00069 | 0.560 |
MOD_Plk_1 | 516 | 522 | PF00069 | 0.493 |
MOD_Plk_4 | 227 | 233 | PF00069 | 0.442 |
MOD_Plk_4 | 362 | 368 | PF00069 | 0.365 |
MOD_ProDKin_1 | 423 | 429 | PF00069 | 0.659 |
MOD_ProDKin_1 | 83 | 89 | PF00069 | 0.702 |
MOD_SUMO_for_1 | 176 | 179 | PF00179 | 0.612 |
MOD_SUMO_for_1 | 209 | 212 | PF00179 | 0.632 |
MOD_SUMO_for_1 | 278 | 281 | PF00179 | 0.548 |
MOD_SUMO_for_1 | 521 | 524 | PF00179 | 0.491 |
MOD_SUMO_rev_2 | 155 | 164 | PF00179 | 0.474 |
TRG_AP2beta_CARGO_1 | 127 | 137 | PF09066 | 0.405 |
TRG_DiLeu_BaEn_1 | 524 | 529 | PF01217 | 0.600 |
TRG_DiLeu_BaLyEn_6 | 257 | 262 | PF01217 | 0.424 |
TRG_ENDOCYTIC_2 | 147 | 150 | PF00928 | 0.562 |
TRG_ENDOCYTIC_2 | 231 | 234 | PF00928 | 0.568 |
TRG_ENDOCYTIC_2 | 333 | 336 | PF00928 | 0.392 |
TRG_ENDOCYTIC_2 | 350 | 353 | PF00928 | 0.374 |
TRG_ENDOCYTIC_2 | 476 | 479 | PF00928 | 0.548 |
TRG_ER_diArg_1 | 136 | 139 | PF00400 | 0.507 |
TRG_ER_diArg_1 | 254 | 257 | PF00400 | 0.454 |
TRG_ER_diArg_1 | 337 | 339 | PF00400 | 0.347 |
TRG_ER_diArg_1 | 412 | 414 | PF00400 | 0.530 |
TRG_ER_diArg_1 | 512 | 514 | PF00400 | 0.476 |
TRG_ER_diArg_1 | 87 | 89 | PF00400 | 0.674 |
TRG_Pf-PMV_PEXEL_1 | 200 | 204 | PF00026 | 0.489 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P368 | Leptomonas seymouri | 61% | 89% |
A0A0S4JFA6 | Bodo saltans | 37% | 88% |
A0A1X0NXZ0 | Trypanosomatidae | 43% | 82% |
A0A3Q8IB76 | Leishmania donovani | 92% | 100% |
A0A422NSQ1 | Trypanosoma rangeli | 44% | 89% |
A4HBY7 | Leishmania braziliensis | 81% | 86% |
A4HZC8 | Leishmania infantum | 92% | 100% |
D0A156 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 92% |
E9AVB5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
V5BLU1 | Trypanosoma cruzi | 42% | 91% |