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: E9ASR2
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043169 | cation binding | 3 | 11 |
GO:0046872 | metal ion binding | 4 | 11 |
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003723 | RNA binding | 4 | 1 |
GO:0003729 | mRNA binding | 5 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 119 | 121 | PF00675 | 0.574 |
CLV_NRD_NRD_1 | 175 | 177 | PF00675 | 0.576 |
CLV_NRD_NRD_1 | 257 | 259 | PF00675 | 0.582 |
CLV_NRD_NRD_1 | 26 | 28 | PF00675 | 0.673 |
CLV_NRD_NRD_1 | 407 | 409 | PF00675 | 0.447 |
CLV_NRD_NRD_1 | 542 | 544 | PF00675 | 0.392 |
CLV_NRD_NRD_1 | 555 | 557 | PF00675 | 0.551 |
CLV_NRD_NRD_1 | 89 | 91 | PF00675 | 0.600 |
CLV_PCSK_KEX2_1 | 175 | 177 | PF00082 | 0.605 |
CLV_PCSK_KEX2_1 | 257 | 259 | PF00082 | 0.638 |
CLV_PCSK_KEX2_1 | 26 | 28 | PF00082 | 0.526 |
CLV_PCSK_KEX2_1 | 407 | 409 | PF00082 | 0.447 |
CLV_PCSK_SKI1_1 | 11 | 15 | PF00082 | 0.589 |
CLV_PCSK_SKI1_1 | 175 | 179 | PF00082 | 0.549 |
CLV_PCSK_SKI1_1 | 180 | 184 | PF00082 | 0.472 |
CLV_PCSK_SKI1_1 | 231 | 235 | PF00082 | 0.666 |
CLV_PCSK_SKI1_1 | 265 | 269 | PF00082 | 0.502 |
CLV_PCSK_SKI1_1 | 544 | 548 | PF00082 | 0.565 |
CLV_PCSK_SKI1_1 | 557 | 561 | PF00082 | 0.593 |
CLV_Separin_Metazoa | 172 | 176 | PF03568 | 0.605 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.548 |
DOC_CKS1_1 | 21 | 26 | PF01111 | 0.669 |
DOC_CYCLIN_yCln2_LP_2 | 233 | 239 | PF00134 | 0.518 |
DOC_MAPK_gen_1 | 257 | 266 | PF00069 | 0.542 |
DOC_MAPK_HePTP_8 | 254 | 266 | PF00069 | 0.423 |
DOC_MAPK_MEF2A_6 | 257 | 266 | PF00069 | 0.423 |
DOC_MAPK_MEF2A_6 | 54 | 63 | PF00069 | 0.540 |
DOC_PP2B_LxvP_1 | 233 | 236 | PF13499 | 0.671 |
DOC_PP2B_LxvP_1 | 59 | 62 | PF13499 | 0.415 |
DOC_PP4_FxxP_1 | 18 | 21 | PF00568 | 0.423 |
DOC_PP4_FxxP_1 | 203 | 206 | PF00568 | 0.676 |
DOC_PP4_FxxP_1 | 426 | 429 | PF00568 | 0.485 |
DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.375 |
DOC_USP7_MATH_1 | 419 | 423 | PF00917 | 0.501 |
DOC_USP7_MATH_1 | 438 | 442 | PF00917 | 0.475 |
DOC_USP7_MATH_1 | 78 | 82 | PF00917 | 0.570 |
DOC_USP7_UBL2_3 | 525 | 529 | PF12436 | 0.363 |
DOC_WW_Pin1_4 | 20 | 25 | PF00397 | 0.677 |
DOC_WW_Pin1_4 | 249 | 254 | PF00397 | 0.648 |
DOC_WW_Pin1_4 | 305 | 310 | PF00397 | 0.528 |
DOC_WW_Pin1_4 | 413 | 418 | PF00397 | 0.475 |
DOC_WW_Pin1_4 | 487 | 492 | PF00397 | 0.687 |
LIG_14-3-3_CanoR_1 | 175 | 184 | PF00244 | 0.542 |
LIG_14-3-3_CanoR_1 | 26 | 31 | PF00244 | 0.672 |
LIG_14-3-3_CanoR_1 | 285 | 294 | PF00244 | 0.564 |
LIG_14-3-3_CanoR_1 | 418 | 426 | PF00244 | 0.449 |
LIG_14-3-3_CanoR_1 | 476 | 484 | PF00244 | 0.644 |
LIG_14-3-3_CanoR_1 | 54 | 60 | PF00244 | 0.671 |
LIG_14-3-3_CanoR_1 | 551 | 556 | PF00244 | 0.666 |
LIG_14-3-3_CanoR_1 | 64 | 68 | PF00244 | 0.571 |
LIG_BRCT_BRCA1_1 | 131 | 135 | PF00533 | 0.431 |
LIG_BRCT_BRCA1_1 | 325 | 329 | PF00533 | 0.466 |
LIG_BRCT_BRCA1_1 | 35 | 39 | PF00533 | 0.671 |
LIG_BRCT_BRCA1_1 | 527 | 531 | PF00533 | 0.348 |
LIG_CSL_BTD_1 | 21 | 24 | PF09270 | 0.615 |
LIG_FHA_1 | 345 | 351 | PF00498 | 0.558 |
LIG_FHA_1 | 56 | 62 | PF00498 | 0.615 |
LIG_FHA_2 | 195 | 201 | PF00498 | 0.637 |
LIG_FHA_2 | 306 | 312 | PF00498 | 0.493 |
LIG_FHA_2 | 367 | 373 | PF00498 | 0.675 |
LIG_FHA_2 | 389 | 395 | PF00498 | 0.543 |
LIG_FHA_2 | 465 | 471 | PF00498 | 0.575 |
LIG_HOMEOBOX | 280 | 283 | PF00046 | 0.470 |
LIG_LIR_Apic_2 | 200 | 206 | PF02991 | 0.666 |
LIG_LIR_Apic_2 | 311 | 315 | PF02991 | 0.557 |
LIG_LIR_Apic_2 | 423 | 429 | PF02991 | 0.475 |
LIG_LIR_Gen_1 | 189 | 199 | PF02991 | 0.512 |
LIG_LIR_Nem_3 | 113 | 119 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 189 | 194 | PF02991 | 0.497 |
LIG_PDZ_Class_2 | 556 | 561 | PF00595 | 0.620 |
LIG_Pex14_1 | 455 | 459 | PF04695 | 0.592 |
LIG_Pex14_2 | 18 | 22 | PF04695 | 0.572 |
LIG_SH2_CRK | 116 | 120 | PF00017 | 0.484 |
LIG_SH2_CRK | 56 | 60 | PF00017 | 0.726 |
LIG_SH2_NCK_1 | 161 | 165 | PF00017 | 0.380 |
LIG_SH2_NCK_1 | 196 | 200 | PF00017 | 0.646 |
LIG_SH2_STAP1 | 527 | 531 | PF00017 | 0.449 |
LIG_SH2_STAT3 | 384 | 387 | PF00017 | 0.754 |
LIG_SH2_STAT5 | 196 | 199 | PF00017 | 0.587 |
LIG_SH2_STAT5 | 330 | 333 | PF00017 | 0.532 |
LIG_SH2_STAT5 | 384 | 387 | PF00017 | 0.754 |
LIG_SH2_STAT5 | 396 | 399 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 459 | 462 | PF00017 | 0.594 |
LIG_SH2_STAT5 | 56 | 59 | PF00017 | 0.704 |
LIG_SH3_2 | 21 | 26 | PF14604 | 0.482 |
LIG_SH3_3 | 18 | 24 | PF00018 | 0.671 |
LIG_SH3_3 | 271 | 277 | PF00018 | 0.601 |
LIG_SH3_3 | 361 | 367 | PF00018 | 0.337 |
LIG_SH3_3 | 443 | 449 | PF00018 | 0.731 |
LIG_SH3_3 | 552 | 558 | PF00018 | 0.610 |
LIG_TRAF2_1 | 169 | 172 | PF00917 | 0.549 |
LIG_TYR_ITIM | 114 | 119 | PF00017 | 0.461 |
MOD_CDK_SPK_2 | 413 | 418 | PF00069 | 0.475 |
MOD_CDK_SPxK_1 | 20 | 26 | PF00069 | 0.486 |
MOD_CDK_SPxxK_3 | 20 | 27 | PF00069 | 0.623 |
MOD_CK1_1 | 129 | 135 | PF00069 | 0.494 |
MOD_CK1_1 | 33 | 39 | PF00069 | 0.623 |
MOD_CK1_1 | 406 | 412 | PF00069 | 0.362 |
MOD_CK1_1 | 514 | 520 | PF00069 | 0.671 |
MOD_CK1_1 | 550 | 556 | PF00069 | 0.572 |
MOD_CK1_1 | 66 | 72 | PF00069 | 0.651 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.474 |
MOD_CK2_1 | 164 | 170 | PF00069 | 0.460 |
MOD_CK2_1 | 192 | 198 | PF00069 | 0.505 |
MOD_CK2_1 | 305 | 311 | PF00069 | 0.515 |
MOD_CK2_1 | 366 | 372 | PF00069 | 0.678 |
MOD_CK2_1 | 388 | 394 | PF00069 | 0.502 |
MOD_CK2_1 | 514 | 520 | PF00069 | 0.489 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.650 |
MOD_GlcNHglycan | 430 | 433 | PF01048 | 0.779 |
MOD_GlcNHglycan | 439 | 443 | PF01048 | 0.612 |
MOD_GlcNHglycan | 46 | 49 | PF01048 | 0.692 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.692 |
MOD_GlcNHglycan | 547 | 550 | PF01048 | 0.655 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.543 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.668 |
MOD_GSK3_1 | 460 | 467 | PF00069 | 0.455 |
MOD_GSK3_1 | 483 | 490 | PF00069 | 0.700 |
MOD_GSK3_1 | 507 | 514 | PF00069 | 0.567 |
MOD_GSK3_1 | 547 | 554 | PF00069 | 0.668 |
MOD_N-GLC_1 | 285 | 290 | PF02516 | 0.603 |
MOD_N-GLC_1 | 388 | 393 | PF02516 | 0.515 |
MOD_N-GLC_1 | 403 | 408 | PF02516 | 0.449 |
MOD_N-GLC_2 | 153 | 155 | PF02516 | 0.385 |
MOD_NEK2_1 | 30 | 35 | PF00069 | 0.679 |
MOD_NEK2_1 | 316 | 321 | PF00069 | 0.460 |
MOD_NEK2_1 | 323 | 328 | PF00069 | 0.441 |
MOD_NEK2_1 | 403 | 408 | PF00069 | 0.449 |
MOD_NEK2_1 | 412 | 417 | PF00069 | 0.449 |
MOD_NEK2_1 | 49 | 54 | PF00069 | 0.639 |
MOD_NEK2_1 | 547 | 552 | PF00069 | 0.488 |
MOD_NEK2_1 | 63 | 68 | PF00069 | 0.538 |
MOD_NEK2_2 | 346 | 351 | PF00069 | 0.427 |
MOD_NEK2_2 | 78 | 83 | PF00069 | 0.550 |
MOD_OFUCOSY | 284 | 289 | PF10250 | 0.487 |
MOD_OFUCOSY | 77 | 82 | PF10250 | 0.559 |
MOD_PIKK_1 | 483 | 489 | PF00454 | 0.644 |
MOD_PK_1 | 551 | 557 | PF00069 | 0.669 |
MOD_PKA_1 | 175 | 181 | PF00069 | 0.549 |
MOD_PKA_1 | 26 | 32 | PF00069 | 0.422 |
MOD_PKA_2 | 175 | 181 | PF00069 | 0.566 |
MOD_PKA_2 | 26 | 32 | PF00069 | 0.713 |
MOD_PKA_2 | 284 | 290 | PF00069 | 0.542 |
MOD_PKA_2 | 406 | 412 | PF00069 | 0.388 |
MOD_PKA_2 | 475 | 481 | PF00069 | 0.516 |
MOD_PKA_2 | 550 | 556 | PF00069 | 0.702 |
MOD_PKA_2 | 63 | 69 | PF00069 | 0.648 |
MOD_Plk_1 | 296 | 302 | PF00069 | 0.553 |
MOD_Plk_2-3 | 192 | 198 | PF00069 | 0.625 |
MOD_Plk_2-3 | 366 | 372 | PF00069 | 0.645 |
MOD_Plk_4 | 26 | 32 | PF00069 | 0.677 |
MOD_Plk_4 | 346 | 352 | PF00069 | 0.468 |
MOD_ProDKin_1 | 20 | 26 | PF00069 | 0.678 |
MOD_ProDKin_1 | 249 | 255 | PF00069 | 0.641 |
MOD_ProDKin_1 | 305 | 311 | PF00069 | 0.528 |
MOD_ProDKin_1 | 413 | 419 | PF00069 | 0.475 |
MOD_ProDKin_1 | 487 | 493 | PF00069 | 0.690 |
MOD_SUMO_rev_2 | 361 | 370 | PF00179 | 0.360 |
TRG_DiLeu_BaEn_1 | 179 | 184 | PF01217 | 0.321 |
TRG_DiLeu_BaEn_1 | 99 | 104 | PF01217 | 0.583 |
TRG_ENDOCYTIC_2 | 116 | 119 | PF00928 | 0.481 |
TRG_ENDOCYTIC_2 | 56 | 59 | PF00928 | 0.706 |
TRG_ER_diArg_1 | 174 | 176 | PF00400 | 0.602 |
TRG_ER_diArg_1 | 25 | 27 | PF00400 | 0.669 |
TRG_ER_diArg_1 | 465 | 468 | PF00400 | 0.480 |
TRG_ER_diArg_1 | 531 | 534 | PF00400 | 0.482 |
TRG_NLS_MonoExtC_3 | 119 | 124 | PF00514 | 0.566 |
TRG_Pf-PMV_PEXEL_1 | 368 | 372 | PF00026 | 0.537 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3U7 | Leptomonas seymouri | 54% | 98% |
A0A0S4JG42 | Bodo saltans | 39% | 100% |
A0A1X0P892 | Trypanosomatidae | 46% | 100% |
A0A3R7KC50 | Trypanosoma rangeli | 47% | 100% |
A0A3S7XAK2 | Leishmania donovani | 89% | 100% |
A4HP02 | Leishmania braziliensis | 75% | 100% |
A4ICJ4 | Leishmania infantum | 89% | 100% |
D0A2X8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 100% |
Q4Q1T4 | Leishmania major | 90% | 100% |
V5BJY2 | Trypanosoma cruzi | 46% | 100% |