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: A4HGC7
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003723 | RNA binding | 4 | 1 |
GO:0005488 | binding | 1 | 3 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
GO:0043167 | ion binding | 2 | 2 |
GO:0043169 | cation binding | 3 | 2 |
GO:0046872 | metal ion binding | 4 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 111 | 115 | PF00656 | 0.670 |
CLV_NRD_NRD_1 | 135 | 137 | PF00675 | 0.463 |
CLV_NRD_NRD_1 | 373 | 375 | PF00675 | 0.545 |
CLV_NRD_NRD_1 | 495 | 497 | PF00675 | 0.515 |
CLV_NRD_NRD_1 | 499 | 501 | PF00675 | 0.500 |
CLV_PCSK_KEX2_1 | 135 | 137 | PF00082 | 0.463 |
CLV_PCSK_KEX2_1 | 375 | 377 | PF00082 | 0.521 |
CLV_PCSK_KEX2_1 | 495 | 497 | PF00082 | 0.517 |
CLV_PCSK_KEX2_1 | 499 | 501 | PF00082 | 0.496 |
CLV_PCSK_PC1ET2_1 | 375 | 377 | PF00082 | 0.571 |
CLV_PCSK_PC7_1 | 495 | 501 | PF00082 | 0.500 |
CLV_PCSK_SKI1_1 | 293 | 297 | PF00082 | 0.508 |
DEG_APCC_DBOX_1 | 292 | 300 | PF00400 | 0.447 |
DEG_SCF_FBW7_1 | 521 | 528 | PF00400 | 0.559 |
DOC_CDC14_PxL_1 | 20 | 28 | PF14671 | 0.755 |
DOC_CKS1_1 | 160 | 165 | PF01111 | 0.570 |
DOC_CYCLIN_RxL_1 | 290 | 298 | PF00134 | 0.542 |
DOC_CYCLIN_yCln2_LP_2 | 320 | 326 | PF00134 | 0.496 |
DOC_MAPK_DCC_7 | 16 | 25 | PF00069 | 0.751 |
DOC_MAPK_DCC_7 | 522 | 531 | PF00069 | 0.418 |
DOC_MAPK_gen_1 | 13 | 22 | PF00069 | 0.717 |
DOC_MAPK_gen_1 | 374 | 382 | PF00069 | 0.300 |
DOC_MAPK_gen_1 | 406 | 413 | PF00069 | 0.477 |
DOC_MAPK_gen_1 | 441 | 450 | PF00069 | 0.593 |
DOC_MAPK_HePTP_8 | 403 | 415 | PF00069 | 0.351 |
DOC_MAPK_MEF2A_6 | 16 | 25 | PF00069 | 0.751 |
DOC_MAPK_MEF2A_6 | 406 | 415 | PF00069 | 0.550 |
DOC_MAPK_MEF2A_6 | 458 | 467 | PF00069 | 0.524 |
DOC_MAPK_MEF2A_6 | 522 | 531 | PF00069 | 0.414 |
DOC_PP4_FxxP_1 | 300 | 303 | PF00568 | 0.497 |
DOC_USP7_MATH_1 | 154 | 158 | PF00917 | 0.555 |
DOC_USP7_MATH_1 | 329 | 333 | PF00917 | 0.441 |
DOC_USP7_MATH_1 | 378 | 382 | PF00917 | 0.485 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.546 |
DOC_USP7_MATH_1 | 437 | 441 | PF00917 | 0.602 |
DOC_USP7_MATH_1 | 525 | 529 | PF00917 | 0.587 |
DOC_USP7_MATH_2 | 31 | 37 | PF00917 | 0.693 |
DOC_USP7_UBL2_3 | 483 | 487 | PF12436 | 0.514 |
DOC_WW_Pin1_4 | 135 | 140 | PF00397 | 0.512 |
DOC_WW_Pin1_4 | 144 | 149 | PF00397 | 0.471 |
DOC_WW_Pin1_4 | 159 | 164 | PF00397 | 0.509 |
DOC_WW_Pin1_4 | 319 | 324 | PF00397 | 0.399 |
DOC_WW_Pin1_4 | 41 | 46 | PF00397 | 0.675 |
DOC_WW_Pin1_4 | 521 | 526 | PF00397 | 0.479 |
DOC_WW_Pin1_4 | 54 | 59 | PF00397 | 0.681 |
DOC_WW_Pin1_4 | 72 | 77 | PF00397 | 0.495 |
DOC_WW_Pin1_4 | 85 | 90 | PF00397 | 0.503 |
LIG_14-3-3_CanoR_1 | 204 | 212 | PF00244 | 0.540 |
LIG_14-3-3_CanoR_1 | 214 | 222 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 257 | 261 | PF00244 | 0.465 |
LIG_14-3-3_CanoR_1 | 80 | 89 | PF00244 | 0.605 |
LIG_Actin_WH2_2 | 263 | 278 | PF00022 | 0.255 |
LIG_APCC_ABBA_1 | 189 | 194 | PF00400 | 0.545 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.703 |
LIG_BRCT_BRCA1_1 | 185 | 189 | PF00533 | 0.521 |
LIG_BRCT_BRCA1_1 | 446 | 450 | PF00533 | 0.408 |
LIG_deltaCOP1_diTrp_1 | 368 | 377 | PF00928 | 0.539 |
LIG_deltaCOP1_diTrp_1 | 475 | 478 | PF00928 | 0.390 |
LIG_EH1_1 | 268 | 276 | PF00400 | 0.483 |
LIG_EH1_1 | 308 | 316 | PF00400 | 0.528 |
LIG_FHA_1 | 122 | 128 | PF00498 | 0.432 |
LIG_FHA_1 | 266 | 272 | PF00498 | 0.412 |
LIG_FHA_1 | 392 | 398 | PF00498 | 0.546 |
LIG_FHA_1 | 406 | 412 | PF00498 | 0.467 |
LIG_FHA_1 | 460 | 466 | PF00498 | 0.398 |
LIG_FHA_1 | 513 | 519 | PF00498 | 0.410 |
LIG_FHA_1 | 72 | 78 | PF00498 | 0.620 |
LIG_FHA_1 | 85 | 91 | PF00498 | 0.780 |
LIG_FHA_1 | 98 | 104 | PF00498 | 0.690 |
LIG_FHA_2 | 285 | 291 | PF00498 | 0.456 |
LIG_FHA_2 | 55 | 61 | PF00498 | 0.792 |
LIG_IRF3_LxIS_1 | 123 | 128 | PF10401 | 0.506 |
LIG_LIR_Apic_2 | 298 | 303 | PF02991 | 0.512 |
LIG_LIR_Gen_1 | 259 | 267 | PF02991 | 0.268 |
LIG_LIR_Gen_1 | 354 | 365 | PF02991 | 0.392 |
LIG_LIR_Gen_1 | 379 | 390 | PF02991 | 0.478 |
LIG_LIR_Gen_1 | 447 | 456 | PF02991 | 0.388 |
LIG_LIR_Gen_1 | 475 | 486 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 124 | 129 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 259 | 263 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 280 | 285 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 290 | 295 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 336 | 340 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 354 | 360 | PF02991 | 0.172 |
LIG_LIR_Nem_3 | 379 | 385 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 447 | 453 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 46 | 51 | PF02991 | 0.540 |
LIG_LIR_Nem_3 | 475 | 481 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 484 | 489 | PF02991 | 0.386 |
LIG_MYND_1 | 159 | 163 | PF01753 | 0.522 |
LIG_Pex14_2 | 260 | 264 | PF04695 | 0.404 |
LIG_PTB_Apo_2 | 310 | 317 | PF02174 | 0.475 |
LIG_SH2_CRK | 292 | 296 | PF00017 | 0.521 |
LIG_SH2_CRK | 486 | 490 | PF00017 | 0.426 |
LIG_SH2_SRC | 352 | 355 | PF00017 | 0.370 |
LIG_SH2_STAP1 | 176 | 180 | PF00017 | 0.283 |
LIG_SH2_STAP1 | 409 | 413 | PF00017 | 0.389 |
LIG_SH2_STAT3 | 131 | 134 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 126 | 129 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 150 | 153 | PF00017 | 0.641 |
LIG_SH2_STAT5 | 266 | 269 | PF00017 | 0.308 |
LIG_SH2_STAT5 | 352 | 355 | PF00017 | 0.370 |
LIG_SH2_STAT5 | 456 | 459 | PF00017 | 0.381 |
LIG_SH2_STAT5 | 466 | 469 | PF00017 | 0.390 |
LIG_SH3_3 | 148 | 154 | PF00018 | 0.571 |
LIG_SH3_3 | 18 | 24 | PF00018 | 0.725 |
LIG_SUMO_SIM_anti_2 | 429 | 434 | PF11976 | 0.392 |
LIG_SUMO_SIM_par_1 | 341 | 348 | PF11976 | 0.406 |
LIG_SUMO_SIM_par_1 | 417 | 423 | PF11976 | 0.486 |
LIG_TRAF2_1 | 207 | 210 | PF00917 | 0.485 |
LIG_TRAF2_1 | 365 | 368 | PF00917 | 0.344 |
LIG_UBA3_1 | 160 | 166 | PF00899 | 0.608 |
LIG_UBA3_1 | 295 | 301 | PF00899 | 0.513 |
MOD_CDK_SPxxK_3 | 159 | 166 | PF00069 | 0.590 |
MOD_CK1_1 | 196 | 202 | PF00069 | 0.546 |
MOD_CK1_1 | 319 | 325 | PF00069 | 0.397 |
MOD_CK1_1 | 345 | 351 | PF00069 | 0.365 |
MOD_CK1_1 | 38 | 44 | PF00069 | 0.769 |
MOD_CK1_1 | 420 | 426 | PF00069 | 0.447 |
MOD_CK1_1 | 54 | 60 | PF00069 | 0.495 |
MOD_CK1_1 | 84 | 90 | PF00069 | 0.817 |
MOD_CK1_1 | 97 | 103 | PF00069 | 0.649 |
MOD_CK2_1 | 204 | 210 | PF00069 | 0.506 |
MOD_GlcNHglycan | 185 | 188 | PF01048 | 0.542 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.433 |
MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.503 |
MOD_GlcNHglycan | 235 | 238 | PF01048 | 0.433 |
MOD_GlcNHglycan | 347 | 350 | PF01048 | 0.397 |
MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.803 |
MOD_GlcNHglycan | 96 | 99 | PF01048 | 0.747 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.459 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.796 |
MOD_GSK3_1 | 407 | 414 | PF00069 | 0.412 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.791 |
MOD_GSK3_1 | 521 | 528 | PF00069 | 0.559 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.720 |
MOD_N-GLC_1 | 512 | 517 | PF02516 | 0.428 |
MOD_N-GLC_1 | 80 | 85 | PF02516 | 0.757 |
MOD_NEK2_1 | 125 | 130 | PF00069 | 0.465 |
MOD_NEK2_1 | 316 | 321 | PF00069 | 0.385 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.701 |
MOD_NEK2_1 | 405 | 410 | PF00069 | 0.539 |
MOD_NEK2_1 | 481 | 486 | PF00069 | 0.418 |
MOD_NEK2_1 | 51 | 56 | PF00069 | 0.603 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.462 |
MOD_NEK2_2 | 121 | 126 | PF00069 | 0.442 |
MOD_PIKK_1 | 102 | 108 | PF00454 | 0.621 |
MOD_PIKK_1 | 213 | 219 | PF00454 | 0.560 |
MOD_PIKK_1 | 4 | 10 | PF00454 | 0.539 |
MOD_PK_1 | 16 | 22 | PF00069 | 0.644 |
MOD_PK_1 | 407 | 413 | PF00069 | 0.549 |
MOD_PKA_2 | 213 | 219 | PF00069 | 0.492 |
MOD_PKA_2 | 256 | 262 | PF00069 | 0.462 |
MOD_PKA_2 | 79 | 85 | PF00069 | 0.781 |
MOD_PKB_1 | 374 | 382 | PF00069 | 0.496 |
MOD_PKB_1 | 441 | 449 | PF00069 | 0.567 |
MOD_Plk_1 | 391 | 397 | PF00069 | 0.292 |
MOD_Plk_1 | 443 | 449 | PF00069 | 0.431 |
MOD_Plk_1 | 512 | 518 | PF00069 | 0.437 |
MOD_Plk_4 | 121 | 127 | PF00069 | 0.468 |
MOD_Plk_4 | 256 | 262 | PF00069 | 0.430 |
MOD_Plk_4 | 329 | 335 | PF00069 | 0.446 |
MOD_Plk_4 | 426 | 432 | PF00069 | 0.422 |
MOD_Plk_4 | 459 | 465 | PF00069 | 0.490 |
MOD_Plk_4 | 481 | 487 | PF00069 | 0.435 |
MOD_ProDKin_1 | 135 | 141 | PF00069 | 0.508 |
MOD_ProDKin_1 | 144 | 150 | PF00069 | 0.467 |
MOD_ProDKin_1 | 159 | 165 | PF00069 | 0.508 |
MOD_ProDKin_1 | 319 | 325 | PF00069 | 0.397 |
MOD_ProDKin_1 | 41 | 47 | PF00069 | 0.676 |
MOD_ProDKin_1 | 521 | 527 | PF00069 | 0.486 |
MOD_ProDKin_1 | 54 | 60 | PF00069 | 0.682 |
MOD_ProDKin_1 | 72 | 78 | PF00069 | 0.493 |
MOD_ProDKin_1 | 85 | 91 | PF00069 | 0.502 |
MOD_SUMO_rev_2 | 368 | 377 | PF00179 | 0.352 |
TRG_DiLeu_BaEn_4 | 210 | 216 | PF01217 | 0.523 |
TRG_ENDOCYTIC_2 | 176 | 179 | PF00928 | 0.538 |
TRG_ENDOCYTIC_2 | 235 | 238 | PF00928 | 0.438 |
TRG_ENDOCYTIC_2 | 292 | 295 | PF00928 | 0.417 |
TRG_ENDOCYTIC_2 | 485 | 488 | PF00928 | 0.408 |
TRG_ER_diArg_1 | 374 | 377 | PF00400 | 0.477 |
TRG_ER_diArg_1 | 494 | 496 | PF00400 | 0.495 |
TRG_ER_diArg_1 | 498 | 500 | PF00400 | 0.496 |
TRG_ER_diArg_1 | 519 | 522 | PF00400 | 0.463 |
TRG_Pf-PMV_PEXEL_1 | 293 | 298 | PF00026 | 0.524 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I6Z5 | Leptomonas seymouri | 68% | 100% |
A0A0S4IP32 | Bodo saltans | 40% | 100% |
A0A1X0NYG7 | Trypanosomatidae | 52% | 100% |
A0A3Q8IDT7 | Leishmania donovani | 86% | 100% |
A0A3R7LMJ5 | Trypanosoma rangeli | 54% | 100% |
A4I3F9 | Leishmania infantum | 85% | 100% |
D0A7X9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 53% | 100% |
E9AZP8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
Q4Q8I5 | Leishmania major | 85% | 100% |
V5DH50 | Trypanosoma cruzi | 54% | 100% |