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:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9B6F5
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005525 | GTP binding | 5 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0019001 | guanyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032561 | guanyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 319 | 323 | PF00656 | 0.759 |
CLV_NRD_NRD_1 | 115 | 117 | PF00675 | 0.274 |
CLV_NRD_NRD_1 | 219 | 221 | PF00675 | 0.441 |
CLV_NRD_NRD_1 | 24 | 26 | PF00675 | 0.591 |
CLV_NRD_NRD_1 | 486 | 488 | PF00675 | 0.594 |
CLV_NRD_NRD_1 | 492 | 494 | PF00675 | 0.616 |
CLV_PCSK_KEX2_1 | 115 | 117 | PF00082 | 0.276 |
CLV_PCSK_KEX2_1 | 23 | 25 | PF00082 | 0.605 |
CLV_PCSK_KEX2_1 | 486 | 488 | PF00082 | 0.594 |
CLV_PCSK_KEX2_1 | 587 | 589 | PF00082 | 0.636 |
CLV_PCSK_PC1ET2_1 | 587 | 589 | PF00082 | 0.666 |
CLV_PCSK_PC7_1 | 19 | 25 | PF00082 | 0.609 |
CLV_PCSK_SKI1_1 | 36 | 40 | PF00082 | 0.712 |
CLV_PCSK_SKI1_1 | 409 | 413 | PF00082 | 0.523 |
CLV_PCSK_SKI1_1 | 419 | 423 | PF00082 | 0.538 |
CLV_PCSK_SKI1_1 | 427 | 431 | PF00082 | 0.563 |
CLV_PCSK_SKI1_1 | 98 | 102 | PF00082 | 0.276 |
DEG_APCC_DBOX_1 | 426 | 434 | PF00400 | 0.654 |
DEG_ODPH_VHL_1 | 380 | 391 | PF01847 | 0.489 |
DEG_SPOP_SBC_1 | 397 | 401 | PF00917 | 0.721 |
DOC_CKS1_1 | 528 | 533 | PF01111 | 0.696 |
DOC_CKS1_1 | 78 | 83 | PF01111 | 0.476 |
DOC_CYCLIN_RxL_1 | 422 | 434 | PF00134 | 0.658 |
DOC_CYCLIN_RxL_1 | 93 | 103 | PF00134 | 0.500 |
DOC_CYCLIN_yCln2_LP_2 | 603 | 609 | PF00134 | 0.486 |
DOC_MAPK_DCC_7 | 279 | 289 | PF00069 | 0.685 |
DOC_MAPK_gen_1 | 112 | 121 | PF00069 | 0.479 |
DOC_MAPK_MEF2A_6 | 158 | 165 | PF00069 | 0.517 |
DOC_PP1_RVXF_1 | 503 | 510 | PF00149 | 0.597 |
DOC_PP2B_LxvP_1 | 380 | 383 | PF13499 | 0.718 |
DOC_PP2B_LxvP_1 | 596 | 599 | PF13499 | 0.631 |
DOC_PP2B_LxvP_1 | 603 | 606 | PF13499 | 0.637 |
DOC_PP2B_LxvP_1 | 610 | 613 | PF13499 | 0.643 |
DOC_PP4_FxxP_1 | 476 | 479 | PF00568 | 0.537 |
DOC_PP4_FxxP_1 | 485 | 488 | PF00568 | 0.619 |
DOC_USP7_MATH_1 | 362 | 366 | PF00917 | 0.777 |
DOC_USP7_MATH_1 | 397 | 401 | PF00917 | 0.713 |
DOC_USP7_MATH_1 | 492 | 496 | PF00917 | 0.769 |
DOC_USP7_UBL2_3 | 494 | 498 | PF12436 | 0.696 |
DOC_WW_Pin1_4 | 434 | 439 | PF00397 | 0.541 |
DOC_WW_Pin1_4 | 527 | 532 | PF00397 | 0.692 |
DOC_WW_Pin1_4 | 566 | 571 | PF00397 | 0.602 |
DOC_WW_Pin1_4 | 612 | 617 | PF00397 | 0.705 |
DOC_WW_Pin1_4 | 77 | 82 | PF00397 | 0.473 |
LIG_14-3-3_CanoR_1 | 209 | 215 | PF00244 | 0.546 |
LIG_14-3-3_CanoR_1 | 262 | 271 | PF00244 | 0.459 |
LIG_14-3-3_CanoR_1 | 274 | 281 | PF00244 | 0.504 |
LIG_14-3-3_CanoR_1 | 419 | 425 | PF00244 | 0.640 |
LIG_14-3-3_CanoR_1 | 493 | 501 | PF00244 | 0.724 |
LIG_14-3-3_CanoR_1 | 62 | 72 | PF00244 | 0.576 |
LIG_14-3-3_CanoR_1 | 90 | 100 | PF00244 | 0.548 |
LIG_APCC_ABBAyCdc20_2 | 221 | 227 | PF00400 | 0.414 |
LIG_BRCT_BRCA1_1 | 348 | 352 | PF00533 | 0.585 |
LIG_CaM_IQ_9 | 5 | 21 | PF13499 | 0.403 |
LIG_FHA_1 | 195 | 201 | PF00498 | 0.476 |
LIG_FHA_1 | 258 | 264 | PF00498 | 0.480 |
LIG_FHA_1 | 445 | 451 | PF00498 | 0.542 |
LIG_FHA_1 | 78 | 84 | PF00498 | 0.459 |
LIG_FHA_1 | 92 | 98 | PF00498 | 0.446 |
LIG_FHA_2 | 199 | 205 | PF00498 | 0.466 |
LIG_FHA_2 | 262 | 268 | PF00498 | 0.451 |
LIG_FHA_2 | 336 | 342 | PF00498 | 0.648 |
LIG_IBAR_NPY_1 | 468 | 470 | PF08397 | 0.570 |
LIG_LIR_Apic_2 | 436 | 442 | PF02991 | 0.532 |
LIG_LIR_Apic_2 | 482 | 488 | PF02991 | 0.569 |
LIG_LIR_Apic_2 | 586 | 592 | PF02991 | 0.680 |
LIG_LIR_Gen_1 | 140 | 151 | PF02991 | 0.483 |
LIG_LIR_Gen_1 | 222 | 233 | PF02991 | 0.395 |
LIG_LIR_Gen_1 | 245 | 255 | PF02991 | 0.487 |
LIG_LIR_Gen_1 | 530 | 540 | PF02991 | 0.707 |
LIG_LIR_LC3C_4 | 330 | 335 | PF02991 | 0.599 |
LIG_LIR_Nem_3 | 140 | 146 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 222 | 228 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 245 | 251 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 530 | 535 | PF02991 | 0.703 |
LIG_LYPXL_SIV_4 | 416 | 424 | PF13949 | 0.644 |
LIG_PCNA_yPIPBox_3 | 419 | 433 | PF02747 | 0.560 |
LIG_Pex14_2 | 472 | 476 | PF04695 | 0.685 |
LIG_SH2_CRK | 248 | 252 | PF00017 | 0.524 |
LIG_SH2_CRK | 514 | 518 | PF00017 | 0.557 |
LIG_SH2_CRK | 589 | 593 | PF00017 | 0.597 |
LIG_SH2_NCK_1 | 344 | 348 | PF00017 | 0.687 |
LIG_SH2_NCK_1 | 514 | 518 | PF00017 | 0.557 |
LIG_SH2_NCK_1 | 557 | 561 | PF00017 | 0.669 |
LIG_SH2_SRC | 432 | 435 | PF00017 | 0.656 |
LIG_SH2_STAP1 | 248 | 252 | PF00017 | 0.487 |
LIG_SH2_STAP1 | 417 | 421 | PF00017 | 0.611 |
LIG_SH2_STAT3 | 470 | 473 | PF00017 | 0.578 |
LIG_SH2_STAT5 | 168 | 171 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 179 | 182 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 432 | 435 | PF00017 | 0.551 |
LIG_SH2_STAT5 | 470 | 473 | PF00017 | 0.578 |
LIG_SH2_STAT5 | 484 | 487 | PF00017 | 0.581 |
LIG_SH2_STAT5 | 514 | 517 | PF00017 | 0.540 |
LIG_SH2_STAT5 | 518 | 521 | PF00017 | 0.534 |
LIG_SH3_1 | 514 | 520 | PF00018 | 0.538 |
LIG_SH3_3 | 128 | 134 | PF00018 | 0.487 |
LIG_SH3_3 | 384 | 390 | PF00018 | 0.739 |
LIG_SH3_3 | 460 | 466 | PF00018 | 0.596 |
LIG_SH3_3 | 514 | 520 | PF00018 | 0.522 |
LIG_SH3_3 | 603 | 609 | PF00018 | 0.763 |
LIG_SH3_3 | 610 | 616 | PF00018 | 0.783 |
LIG_SH3_3 | 75 | 81 | PF00018 | 0.459 |
LIG_SUMO_SIM_anti_2 | 182 | 187 | PF11976 | 0.487 |
LIG_SUMO_SIM_par_1 | 196 | 201 | PF11976 | 0.476 |
LIG_SUMO_SIM_par_1 | 230 | 236 | PF11976 | 0.420 |
LIG_SxIP_EBH_1 | 397 | 409 | PF03271 | 0.715 |
LIG_TRAF2_1 | 337 | 340 | PF00917 | 0.745 |
LIG_TRAF2_1 | 383 | 386 | PF00917 | 0.657 |
LIG_TRAF2_2 | 291 | 296 | PF00917 | 0.660 |
LIG_TYR_ITIM | 223 | 228 | PF00017 | 0.540 |
LIG_TYR_ITIM | 246 | 251 | PF00017 | 0.507 |
MOD_CDC14_SPxK_1 | 437 | 440 | PF00782 | 0.538 |
MOD_CDK_SPxK_1 | 434 | 440 | PF00069 | 0.540 |
MOD_CK1_1 | 254 | 260 | PF00069 | 0.573 |
MOD_CK1_1 | 399 | 405 | PF00069 | 0.589 |
MOD_CK1_1 | 569 | 575 | PF00069 | 0.463 |
MOD_CK1_1 | 614 | 620 | PF00069 | 0.740 |
MOD_CK2_1 | 100 | 106 | PF00069 | 0.413 |
MOD_CK2_1 | 261 | 267 | PF00069 | 0.466 |
MOD_CK2_1 | 274 | 280 | PF00069 | 0.517 |
MOD_CK2_1 | 335 | 341 | PF00069 | 0.743 |
MOD_CK2_1 | 34 | 40 | PF00069 | 0.698 |
MOD_CK2_1 | 342 | 348 | PF00069 | 0.693 |
MOD_GlcNHglycan | 102 | 105 | PF01048 | 0.473 |
MOD_GlcNHglycan | 143 | 146 | PF01048 | 0.247 |
MOD_GlcNHglycan | 235 | 238 | PF01048 | 0.410 |
MOD_GlcNHglycan | 271 | 274 | PF01048 | 0.586 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.657 |
MOD_GlcNHglycan | 359 | 362 | PF01048 | 0.609 |
MOD_GlcNHglycan | 364 | 367 | PF01048 | 0.577 |
MOD_GlcNHglycan | 65 | 68 | PF01048 | 0.535 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.328 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.328 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.465 |
MOD_GSK3_1 | 342 | 349 | PF00069 | 0.613 |
MOD_GSK3_1 | 612 | 619 | PF00069 | 0.739 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.316 |
MOD_N-GLC_1 | 194 | 199 | PF02516 | 0.328 |
MOD_NEK2_1 | 233 | 238 | PF00069 | 0.411 |
MOD_NEK2_1 | 433 | 438 | PF00069 | 0.391 |
MOD_NEK2_1 | 96 | 101 | PF00069 | 0.310 |
MOD_NEK2_2 | 210 | 215 | PF00069 | 0.559 |
MOD_NEK2_2 | 242 | 247 | PF00069 | 0.468 |
MOD_PIKK_1 | 274 | 280 | PF00454 | 0.520 |
MOD_PIKK_1 | 289 | 295 | PF00454 | 0.576 |
MOD_PIKK_1 | 410 | 416 | PF00454 | 0.608 |
MOD_PIKK_1 | 493 | 499 | PF00454 | 0.729 |
MOD_PIKK_1 | 5 | 11 | PF00454 | 0.403 |
MOD_PIKK_1 | 569 | 575 | PF00454 | 0.502 |
MOD_PKA_1 | 493 | 499 | PF00069 | 0.643 |
MOD_PKA_2 | 261 | 267 | PF00069 | 0.482 |
MOD_PKA_2 | 269 | 275 | PF00069 | 0.490 |
MOD_PKA_2 | 342 | 348 | PF00069 | 0.746 |
MOD_PKA_2 | 492 | 498 | PF00069 | 0.667 |
MOD_PKB_1 | 15 | 23 | PF00069 | 0.696 |
MOD_Plk_1 | 17 | 23 | PF00069 | 0.699 |
MOD_Plk_1 | 194 | 200 | PF00069 | 0.328 |
MOD_Plk_1 | 279 | 285 | PF00069 | 0.655 |
MOD_Plk_1 | 316 | 322 | PF00069 | 0.644 |
MOD_Plk_1 | 372 | 378 | PF00069 | 0.775 |
MOD_Plk_2-3 | 261 | 267 | PF00069 | 0.466 |
MOD_Plk_4 | 372 | 378 | PF00069 | 0.806 |
MOD_Plk_4 | 92 | 98 | PF00069 | 0.328 |
MOD_ProDKin_1 | 434 | 440 | PF00069 | 0.540 |
MOD_ProDKin_1 | 527 | 533 | PF00069 | 0.692 |
MOD_ProDKin_1 | 566 | 572 | PF00069 | 0.600 |
MOD_ProDKin_1 | 612 | 618 | PF00069 | 0.742 |
MOD_ProDKin_1 | 77 | 83 | PF00069 | 0.468 |
TRG_DiLeu_BaEn_1 | 329 | 334 | PF01217 | 0.698 |
TRG_DiLeu_BaLyEn_6 | 425 | 430 | PF01217 | 0.655 |
TRG_DiLeu_BaLyEn_6 | 78 | 83 | PF01217 | 0.277 |
TRG_ENDOCYTIC_2 | 167 | 170 | PF00928 | 0.328 |
TRG_ENDOCYTIC_2 | 225 | 228 | PF00928 | 0.551 |
TRG_ENDOCYTIC_2 | 248 | 251 | PF00928 | 0.514 |
TRG_ENDOCYTIC_2 | 417 | 420 | PF00928 | 0.571 |
TRG_ER_diArg_1 | 114 | 116 | PF00400 | 0.344 |
TRG_ER_diArg_1 | 23 | 25 | PF00400 | 0.622 |
TRG_ER_diArg_1 | 424 | 427 | PF00400 | 0.665 |
TRG_ER_diArg_1 | 485 | 487 | PF00400 | 0.581 |
TRG_Pf-PMV_PEXEL_1 | 112 | 117 | PF00026 | 0.449 |
TRG_Pf-PMV_PEXEL_1 | 36 | 40 | PF00026 | 0.670 |
TRG_Pf-PMV_PEXEL_1 | 427 | 431 | PF00026 | 0.684 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PF63 | Leptomonas seymouri | 70% | 94% |
A0A0S4JFQ6 | Bodo saltans | 48% | 94% |
A0A1X0P5I3 | Trypanosomatidae | 58% | 98% |
A0A3Q8IJ54 | Leishmania donovani | 93% | 100% |
A0A3R7RSH5 | Trypanosoma rangeli | 56% | 97% |
A4HMU2 | Leishmania braziliensis | 85% | 100% |
A4IBE4 | Leishmania infantum | 93% | 100% |
C9ZZ76 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 55% | 98% |
E9AFA0 | Leishmania major | 92% | 100% |
V5C303 | Trypanosoma cruzi | 56% | 91% |