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: A4ICJ4
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003723 | RNA binding | 4 | 1 |
GO:0003729 | mRNA binding | 5 | 1 |
GO:0005488 | binding | 1 | 10 |
GO:0043167 | ion binding | 2 | 10 |
GO:0043169 | cation binding | 3 | 10 |
GO:0046872 | metal ion binding | 4 | 10 |
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 | 0.571 |
CLV_NRD_NRD_1 | 175 | 177 | PF00675 | 0.578 |
CLV_NRD_NRD_1 | 257 | 259 | PF00675 | 0.597 |
CLV_NRD_NRD_1 | 407 | 409 | PF00675 | 0.475 |
CLV_NRD_NRD_1 | 542 | 544 | PF00675 | 0.392 |
CLV_NRD_NRD_1 | 555 | 557 | PF00675 | 0.550 |
CLV_NRD_NRD_1 | 89 | 91 | PF00675 | 0.599 |
CLV_PCSK_KEX2_1 | 175 | 177 | PF00082 | 0.578 |
CLV_PCSK_KEX2_1 | 257 | 259 | PF00082 | 0.652 |
CLV_PCSK_KEX2_1 | 407 | 409 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 175 | 179 | PF00082 | 0.530 |
CLV_PCSK_SKI1_1 | 231 | 235 | PF00082 | 0.591 |
CLV_PCSK_SKI1_1 | 544 | 548 | PF00082 | 0.595 |
CLV_PCSK_SKI1_1 | 557 | 561 | PF00082 | 0.582 |
CLV_Separin_Metazoa | 172 | 176 | PF03568 | 0.583 |
DOC_CKS1_1 | 21 | 26 | PF01111 | 0.685 |
DOC_CYCLIN_RxL_1 | 228 | 236 | PF00134 | 0.484 |
DOC_PP4_FxxP_1 | 203 | 206 | PF00568 | 0.651 |
DOC_USP7_MATH_1 | 549 | 553 | PF00917 | 0.724 |
DOC_USP7_MATH_1 | 78 | 82 | PF00917 | 0.572 |
DOC_USP7_UBL2_3 | 525 | 529 | PF12436 | 0.363 |
DOC_WW_Pin1_4 | 20 | 25 | PF00397 | 0.691 |
DOC_WW_Pin1_4 | 249 | 254 | PF00397 | 0.668 |
DOC_WW_Pin1_4 | 305 | 310 | PF00397 | 0.525 |
DOC_WW_Pin1_4 | 413 | 418 | PF00397 | 0.457 |
DOC_WW_Pin1_4 | 437 | 442 | PF00397 | 0.658 |
DOC_WW_Pin1_4 | 487 | 492 | PF00397 | 0.662 |
LIG_14-3-3_CanoR_1 | 175 | 184 | PF00244 | 0.535 |
LIG_14-3-3_CanoR_1 | 27 | 31 | PF00244 | 0.676 |
LIG_14-3-3_CanoR_1 | 285 | 294 | PF00244 | 0.539 |
LIG_14-3-3_CanoR_1 | 476 | 484 | PF00244 | 0.623 |
LIG_14-3-3_CanoR_1 | 54 | 60 | PF00244 | 0.669 |
LIG_14-3-3_CanoR_1 | 551 | 556 | PF00244 | 0.676 |
LIG_14-3-3_CanoR_1 | 64 | 68 | PF00244 | 0.565 |
LIG_AP2alpha_2 | 428 | 430 | PF02296 | 0.560 |
LIG_BRCT_BRCA1_1 | 131 | 135 | PF00533 | 0.425 |
LIG_BRCT_BRCA1_1 | 325 | 329 | PF00533 | 0.441 |
LIG_BRCT_BRCA1_1 | 527 | 531 | PF00533 | 0.348 |
LIG_CSL_BTD_1 | 21 | 24 | PF09270 | 0.634 |
LIG_FHA_1 | 179 | 185 | PF00498 | 0.497 |
LIG_FHA_1 | 227 | 233 | PF00498 | 0.690 |
LIG_FHA_1 | 345 | 351 | PF00498 | 0.540 |
LIG_FHA_1 | 58 | 64 | PF00498 | 0.600 |
LIG_FHA_1 | 7 | 13 | PF00498 | 0.656 |
LIG_FHA_2 | 195 | 201 | PF00498 | 0.609 |
LIG_FHA_2 | 264 | 270 | PF00498 | 0.719 |
LIG_FHA_2 | 306 | 312 | PF00498 | 0.493 |
LIG_FHA_2 | 367 | 373 | PF00498 | 0.663 |
LIG_FHA_2 | 465 | 471 | PF00498 | 0.562 |
LIG_HOMEOBOX | 280 | 283 | PF00046 | 0.446 |
LIG_LIR_Apic_2 | 200 | 206 | PF02991 | 0.637 |
LIG_LIR_Apic_2 | 311 | 315 | PF02991 | 0.541 |
LIG_LIR_Gen_1 | 189 | 199 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 113 | 119 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 189 | 194 | PF02991 | 0.478 |
LIG_PDZ_Class_2 | 556 | 561 | PF00595 | 0.609 |
LIG_Pex14_1 | 455 | 459 | PF04695 | 0.549 |
LIG_SH2_CRK | 116 | 120 | PF00017 | 0.480 |
LIG_SH2_CRK | 56 | 60 | PF00017 | 0.727 |
LIG_SH2_NCK_1 | 161 | 165 | PF00017 | 0.410 |
LIG_SH2_NCK_1 | 196 | 200 | PF00017 | 0.613 |
LIG_SH2_STAP1 | 527 | 531 | PF00017 | 0.449 |
LIG_SH2_STAT3 | 384 | 387 | PF00017 | 0.720 |
LIG_SH2_STAT5 | 196 | 199 | PF00017 | 0.616 |
LIG_SH2_STAT5 | 330 | 333 | PF00017 | 0.477 |
LIG_SH2_STAT5 | 384 | 387 | PF00017 | 0.729 |
LIG_SH2_STAT5 | 396 | 399 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 459 | 462 | PF00017 | 0.556 |
LIG_SH2_STAT5 | 56 | 59 | PF00017 | 0.693 |
LIG_SH3_3 | 15 | 21 | PF00018 | 0.679 |
LIG_SH3_3 | 271 | 277 | PF00018 | 0.593 |
LIG_SH3_3 | 416 | 422 | PF00018 | 0.453 |
LIG_SH3_3 | 423 | 429 | PF00018 | 0.721 |
LIG_SH3_3 | 443 | 449 | PF00018 | 0.722 |
LIG_SH3_3 | 552 | 558 | PF00018 | 0.617 |
LIG_SH3_CIN85_PxpxPR_1 | 363 | 368 | PF14604 | 0.602 |
LIG_TRAF2_1 | 169 | 172 | PF00917 | 0.558 |
LIG_TYR_ITIM | 114 | 119 | PF00017 | 0.456 |
MOD_CDK_SPK_2 | 413 | 418 | PF00069 | 0.475 |
MOD_CDK_SPxxK_3 | 20 | 27 | PF00069 | 0.636 |
MOD_CK1_1 | 33 | 39 | PF00069 | 0.627 |
MOD_CK1_1 | 406 | 412 | PF00069 | 0.362 |
MOD_CK1_1 | 514 | 520 | PF00069 | 0.475 |
MOD_CK1_1 | 66 | 72 | PF00069 | 0.635 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.496 |
MOD_CK2_1 | 164 | 170 | PF00069 | 0.481 |
MOD_CK2_1 | 192 | 198 | PF00069 | 0.495 |
MOD_CK2_1 | 263 | 269 | PF00069 | 0.708 |
MOD_CK2_1 | 305 | 311 | PF00069 | 0.510 |
MOD_CK2_1 | 366 | 372 | PF00069 | 0.671 |
MOD_GlcNHglycan | 235 | 238 | PF01048 | 0.457 |
MOD_GlcNHglycan | 341 | 344 | PF01048 | 0.464 |
MOD_GlcNHglycan | 430 | 433 | PF01048 | 0.712 |
MOD_GlcNHglycan | 46 | 49 | PF01048 | 0.707 |
MOD_GlcNHglycan | 505 | 508 | PF01048 | 0.700 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.706 |
MOD_GlcNHglycan | 516 | 519 | PF01048 | 0.253 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.544 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.668 |
MOD_GSK3_1 | 460 | 467 | PF00069 | 0.429 |
MOD_GSK3_1 | 483 | 490 | PF00069 | 0.602 |
MOD_GSK3_1 | 547 | 554 | PF00069 | 0.696 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.662 |
MOD_N-GLC_1 | 285 | 290 | PF02516 | 0.586 |
MOD_N-GLC_1 | 403 | 408 | PF02516 | 0.400 |
MOD_N-GLC_1 | 511 | 516 | PF02516 | 0.611 |
MOD_NEK2_1 | 233 | 238 | PF00069 | 0.464 |
MOD_NEK2_1 | 30 | 35 | PF00069 | 0.677 |
MOD_NEK2_1 | 316 | 321 | PF00069 | 0.448 |
MOD_NEK2_1 | 323 | 328 | PF00069 | 0.424 |
MOD_NEK2_1 | 403 | 408 | PF00069 | 0.449 |
MOD_NEK2_1 | 412 | 417 | PF00069 | 0.449 |
MOD_NEK2_1 | 511 | 516 | PF00069 | 0.611 |
MOD_NEK2_1 | 59 | 64 | PF00069 | 0.602 |
MOD_NEK2_2 | 346 | 351 | PF00069 | 0.406 |
MOD_NEK2_2 | 78 | 83 | PF00069 | 0.569 |
MOD_OFUCOSY | 284 | 289 | PF10250 | 0.468 |
MOD_OFUCOSY | 77 | 82 | PF10250 | 0.561 |
MOD_PIKK_1 | 483 | 489 | PF00454 | 0.619 |
MOD_PIKK_1 | 6 | 12 | PF00454 | 0.613 |
MOD_PK_1 | 551 | 557 | PF00069 | 0.676 |
MOD_PKA_1 | 175 | 181 | PF00069 | 0.535 |
MOD_PKA_2 | 175 | 181 | PF00069 | 0.552 |
MOD_PKA_2 | 26 | 32 | PF00069 | 0.713 |
MOD_PKA_2 | 284 | 290 | PF00069 | 0.557 |
MOD_PKA_2 | 406 | 412 | PF00069 | 0.388 |
MOD_PKA_2 | 475 | 481 | PF00069 | 0.529 |
MOD_PKA_2 | 550 | 556 | PF00069 | 0.712 |
MOD_PKA_2 | 63 | 69 | PF00069 | 0.627 |
MOD_Plk_1 | 178 | 184 | PF00069 | 0.595 |
MOD_Plk_1 | 296 | 302 | PF00069 | 0.529 |
MOD_Plk_1 | 511 | 517 | PF00069 | 0.606 |
MOD_Plk_2-3 | 192 | 198 | PF00069 | 0.595 |
MOD_Plk_2-3 | 366 | 372 | PF00069 | 0.638 |
MOD_Plk_4 | 178 | 184 | PF00069 | 0.499 |
MOD_Plk_4 | 26 | 32 | PF00069 | 0.677 |
MOD_Plk_4 | 263 | 269 | PF00069 | 0.698 |
MOD_Plk_4 | 346 | 352 | PF00069 | 0.451 |
MOD_ProDKin_1 | 20 | 26 | PF00069 | 0.692 |
MOD_ProDKin_1 | 249 | 255 | PF00069 | 0.667 |
MOD_ProDKin_1 | 305 | 311 | PF00069 | 0.525 |
MOD_ProDKin_1 | 413 | 419 | PF00069 | 0.457 |
MOD_ProDKin_1 | 437 | 443 | PF00069 | 0.661 |
MOD_ProDKin_1 | 487 | 493 | PF00069 | 0.664 |
TRG_DiLeu_BaEn_1 | 99 | 104 | PF01217 | 0.569 |
TRG_ENDOCYTIC_2 | 116 | 119 | PF00928 | 0.476 |
TRG_ENDOCYTIC_2 | 56 | 59 | PF00928 | 0.710 |
TRG_ER_diArg_1 | 174 | 176 | PF00400 | 0.591 |
TRG_ER_diArg_1 | 465 | 468 | PF00400 | 0.456 |
TRG_ER_diArg_1 | 531 | 534 | PF00400 | 0.482 |
TRG_NLS_MonoExtC_3 | 119 | 124 | PF00514 | 0.562 |
TRG_Pf-PMV_PEXEL_1 | 61 | 65 | PF00026 | 0.650 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3U7 | Leptomonas seymouri | 54% | 98% |
A0A0S4JG42 | Bodo saltans | 38% | 100% |
A0A1X0P892 | Trypanosomatidae | 46% | 100% |
A0A3R7KC50 | Trypanosoma rangeli | 47% | 100% |
A0A3S7XAK2 | Leishmania donovani | 99% | 100% |
A4HP02 | Leishmania braziliensis | 75% | 100% |
D0A2X8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 100% |
E9ASR2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4Q1T4 | Leishmania major | 94% | 100% |
V5BJY2 | Trypanosoma cruzi | 46% | 100% |