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: 3 |
Silverman et al. | no | yes: 3 |
Pissara et al. | yes | yes: 12 |
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: 6 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0043226 | organelle | 2 | 8 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
GO:0005737 | cytoplasm | 2 | 1 |
Related structures:
AlphaFold database: A4HHD6
Term | Name | Level | Count |
---|---|---|---|
GO:0000413 | protein peptidyl-prolyl isomerization | 7 | 1 |
GO:0006457 | protein folding | 2 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0018193 | peptidyl-amino acid modification | 5 | 1 |
GO:0018208 | peptidyl-proline modification | 6 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0061077 | chaperone-mediated protein folding | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 8 |
GO:0005488 | binding | 1 | 8 |
GO:0005524 | ATP binding | 5 | 8 |
GO:0017076 | purine nucleotide binding | 4 | 8 |
GO:0030554 | adenyl nucleotide binding | 5 | 8 |
GO:0032553 | ribonucleotide binding | 3 | 8 |
GO:0032555 | purine ribonucleotide binding | 4 | 8 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 8 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 8 |
GO:0036094 | small molecule binding | 2 | 8 |
GO:0043167 | ion binding | 2 | 8 |
GO:0043168 | anion binding | 3 | 8 |
GO:0044183 | protein folding chaperone | 1 | 8 |
GO:0097159 | organic cyclic compound binding | 2 | 8 |
GO:0097367 | carbohydrate derivative binding | 2 | 8 |
GO:0140657 | ATP-dependent activity | 1 | 8 |
GO:0140662 | ATP-dependent protein folding chaperone | 2 | 8 |
GO:1901265 | nucleoside phosphate binding | 3 | 8 |
GO:1901363 | heterocyclic compound binding | 2 | 8 |
GO:0003755 | peptidyl-prolyl cis-trans isomerase activity | 3 | 1 |
GO:0003824 | catalytic activity | 1 | 1 |
GO:0016853 | isomerase activity | 2 | 1 |
GO:0016859 | cis-trans isomerase activity | 3 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 220 | 224 | PF00656 | 0.333 |
CLV_C14_Caspase3-7 | 419 | 423 | PF00656 | 0.500 |
CLV_C14_Caspase3-7 | 450 | 454 | PF00656 | 0.520 |
CLV_C14_Caspase3-7 | 475 | 479 | PF00656 | 0.353 |
CLV_NRD_NRD_1 | 252 | 254 | PF00675 | 0.346 |
CLV_NRD_NRD_1 | 259 | 261 | PF00675 | 0.311 |
CLV_NRD_NRD_1 | 381 | 383 | PF00675 | 0.486 |
CLV_NRD_NRD_1 | 576 | 578 | PF00675 | 0.447 |
CLV_NRD_NRD_1 | 662 | 664 | PF00675 | 0.335 |
CLV_PCSK_KEX2_1 | 381 | 383 | PF00082 | 0.538 |
CLV_PCSK_KEX2_1 | 575 | 577 | PF00082 | 0.457 |
CLV_PCSK_KEX2_1 | 662 | 664 | PF00082 | 0.330 |
CLV_PCSK_PC1ET2_1 | 575 | 577 | PF00082 | 0.500 |
CLV_PCSK_PC7_1 | 571 | 577 | PF00082 | 0.513 |
CLV_PCSK_SKI1_1 | 106 | 110 | PF00082 | 0.330 |
CLV_PCSK_SKI1_1 | 140 | 144 | PF00082 | 0.429 |
CLV_PCSK_SKI1_1 | 253 | 257 | PF00082 | 0.389 |
CLV_PCSK_SKI1_1 | 260 | 264 | PF00082 | 0.389 |
CLV_PCSK_SKI1_1 | 306 | 310 | PF00082 | 0.494 |
CLV_PCSK_SKI1_1 | 35 | 39 | PF00082 | 0.381 |
CLV_PCSK_SKI1_1 | 352 | 356 | PF00082 | 0.330 |
CLV_PCSK_SKI1_1 | 6 | 10 | PF00082 | 0.370 |
CLV_PCSK_SKI1_1 | 658 | 662 | PF00082 | 0.381 |
CLV_PCSK_SKI1_1 | 701 | 705 | PF00082 | 0.489 |
CLV_PCSK_SKI1_1 | 712 | 716 | PF00082 | 0.444 |
CLV_Separin_Metazoa | 116 | 120 | PF03568 | 0.248 |
CLV_Separin_Metazoa | 331 | 335 | PF03568 | 0.248 |
DEG_APCC_DBOX_1 | 272 | 280 | PF00400 | 0.276 |
DEG_APCC_DBOX_1 | 305 | 313 | PF00400 | 0.389 |
DEG_SPOP_SBC_1 | 265 | 269 | PF00917 | 0.351 |
DOC_ANK_TNKS_1 | 333 | 340 | PF00023 | 0.389 |
DOC_CYCLIN_yCln2_LP_2 | 94 | 100 | PF00134 | 0.406 |
DOC_MAPK_gen_1 | 615 | 623 | PF00069 | 0.430 |
DOC_MAPK_MEF2A_6 | 119 | 127 | PF00069 | 0.406 |
DOC_MAPK_MEF2A_6 | 62 | 70 | PF00069 | 0.406 |
DOC_PP2B_LxvP_1 | 125 | 128 | PF13499 | 0.389 |
DOC_PP2B_LxvP_1 | 316 | 319 | PF13499 | 0.524 |
DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.363 |
DOC_USP7_MATH_1 | 371 | 375 | PF00917 | 0.389 |
DOC_USP7_MATH_1 | 630 | 634 | PF00917 | 0.445 |
DOC_USP7_UBL2_3 | 250 | 254 | PF12436 | 0.330 |
DOC_USP7_UBL2_3 | 708 | 712 | PF12436 | 0.450 |
DOC_USP7_UBL2_3 | 713 | 717 | PF12436 | 0.483 |
DOC_WW_Pin1_4 | 402 | 407 | PF00397 | 0.671 |
DOC_WW_Pin1_4 | 422 | 427 | PF00397 | 0.419 |
DOC_WW_Pin1_4 | 69 | 74 | PF00397 | 0.389 |
LIG_14-3-3_CanoR_1 | 140 | 145 | PF00244 | 0.333 |
LIG_14-3-3_CanoR_1 | 306 | 316 | PF00244 | 0.399 |
LIG_14-3-3_CanoR_1 | 359 | 365 | PF00244 | 0.373 |
LIG_14-3-3_CanoR_1 | 381 | 386 | PF00244 | 0.390 |
LIG_Actin_WH2_2 | 203 | 218 | PF00022 | 0.389 |
LIG_APCC_ABBA_1 | 531 | 536 | PF00400 | 0.371 |
LIG_deltaCOP1_diTrp_1 | 586 | 596 | PF00928 | 0.431 |
LIG_FHA_1 | 118 | 124 | PF00498 | 0.408 |
LIG_FHA_1 | 12 | 18 | PF00498 | 0.389 |
LIG_FHA_1 | 324 | 330 | PF00498 | 0.282 |
LIG_FHA_1 | 508 | 514 | PF00498 | 0.467 |
LIG_FHA_1 | 592 | 598 | PF00498 | 0.410 |
LIG_FHA_1 | 645 | 651 | PF00498 | 0.470 |
LIG_FHA_1 | 692 | 698 | PF00498 | 0.415 |
LIG_FHA_2 | 266 | 272 | PF00498 | 0.389 |
LIG_FHA_2 | 41 | 47 | PF00498 | 0.354 |
LIG_FHA_2 | 414 | 420 | PF00498 | 0.339 |
LIG_FHA_2 | 473 | 479 | PF00498 | 0.350 |
LIG_FHA_2 | 53 | 59 | PF00498 | 0.389 |
LIG_Integrin_RGD_1 | 246 | 248 | PF01839 | 0.389 |
LIG_LIR_Gen_1 | 135 | 144 | PF02991 | 0.398 |
LIG_LIR_Gen_1 | 416 | 426 | PF02991 | 0.341 |
LIG_LIR_Gen_1 | 441 | 449 | PF02991 | 0.505 |
LIG_LIR_Gen_1 | 624 | 634 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 135 | 139 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 228 | 234 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 251 | 255 | PF02991 | 0.330 |
LIG_LIR_Nem_3 | 416 | 421 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 441 | 445 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 525 | 531 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 624 | 629 | PF02991 | 0.427 |
LIG_NRBOX | 104 | 110 | PF00104 | 0.276 |
LIG_Pex14_1 | 50 | 54 | PF04695 | 0.389 |
LIG_Pex14_2 | 715 | 719 | PF04695 | 0.490 |
LIG_Rb_pABgroove_1 | 601 | 609 | PF01858 | 0.455 |
LIG_RPA_C_Fungi | 658 | 670 | PF08784 | 0.389 |
LIG_SH2_CRK | 171 | 175 | PF00017 | 0.389 |
LIG_SH2_CRK | 667 | 671 | PF00017 | 0.406 |
LIG_SH2_GRB2like | 626 | 629 | PF00017 | 0.426 |
LIG_SH2_SRC | 221 | 224 | PF00017 | 0.333 |
LIG_SH2_SRC | 607 | 610 | PF00017 | 0.431 |
LIG_SH2_SRC | 626 | 629 | PF00017 | 0.426 |
LIG_SH2_STAT3 | 469 | 472 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 104 | 107 | PF00017 | 0.428 |
LIG_SH2_STAT5 | 165 | 168 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 221 | 224 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 469 | 472 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 493 | 496 | PF00017 | 0.478 |
LIG_SH2_STAT5 | 500 | 503 | PF00017 | 0.496 |
LIG_SH2_STAT5 | 54 | 57 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 626 | 629 | PF00017 | 0.426 |
LIG_SH3_3 | 651 | 657 | PF00018 | 0.434 |
LIG_SH3_3 | 67 | 73 | PF00018 | 0.389 |
LIG_SUMO_SIM_anti_2 | 282 | 288 | PF11976 | 0.389 |
LIG_SUMO_SIM_par_1 | 183 | 189 | PF11976 | 0.338 |
LIG_SUMO_SIM_par_1 | 284 | 290 | PF11976 | 0.406 |
LIG_TRAF2_1 | 113 | 116 | PF00917 | 0.248 |
LIG_TRAF2_1 | 610 | 613 | PF00917 | 0.556 |
LIG_TYR_ITIM | 169 | 174 | PF00017 | 0.406 |
LIG_TYR_ITIM | 533 | 538 | PF00017 | 0.380 |
LIG_UBA3_1 | 308 | 315 | PF00899 | 0.406 |
LIG_UBA3_1 | 347 | 352 | PF00899 | 0.248 |
LIG_WRC_WIRS_1 | 17 | 22 | PF05994 | 0.389 |
LIG_WRC_WIRS_1 | 249 | 254 | PF05994 | 0.389 |
MOD_CK1_1 | 195 | 201 | PF00069 | 0.398 |
MOD_CK1_1 | 72 | 78 | PF00069 | 0.406 |
MOD_CK2_1 | 24 | 30 | PF00069 | 0.420 |
MOD_CK2_1 | 265 | 271 | PF00069 | 0.389 |
MOD_CK2_1 | 366 | 372 | PF00069 | 0.536 |
MOD_CK2_1 | 413 | 419 | PF00069 | 0.419 |
MOD_CK2_1 | 489 | 495 | PF00069 | 0.409 |
MOD_CK2_1 | 52 | 58 | PF00069 | 0.389 |
MOD_CK2_1 | 534 | 540 | PF00069 | 0.540 |
MOD_CK2_1 | 607 | 613 | PF00069 | 0.557 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.360 |
MOD_GlcNHglycan | 343 | 346 | PF01048 | 0.457 |
MOD_GlcNHglycan | 372 | 376 | PF01048 | 0.389 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.406 |
MOD_GlcNHglycan | 667 | 670 | PF01048 | 0.378 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.398 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.420 |
MOD_GSK3_1 | 265 | 272 | PF00069 | 0.332 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.762 |
MOD_GSK3_1 | 507 | 514 | PF00069 | 0.404 |
MOD_GSK3_1 | 558 | 565 | PF00069 | 0.600 |
MOD_GSK3_1 | 691 | 698 | PF00069 | 0.422 |
MOD_N-GLC_1 | 366 | 371 | PF02516 | 0.406 |
MOD_N-GLC_1 | 613 | 618 | PF02516 | 0.502 |
MOD_N-GLC_1 | 644 | 649 | PF02516 | 0.454 |
MOD_N-GLC_2 | 644 | 646 | PF02516 | 0.461 |
MOD_NEK2_1 | 117 | 122 | PF00069 | 0.385 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.389 |
MOD_NEK2_1 | 355 | 360 | PF00069 | 0.389 |
MOD_NEK2_1 | 421 | 426 | PF00069 | 0.354 |
MOD_NEK2_1 | 52 | 57 | PF00069 | 0.389 |
MOD_NEK2_1 | 82 | 87 | PF00069 | 0.354 |
MOD_NEK2_2 | 534 | 539 | PF00069 | 0.537 |
MOD_NEK2_2 | 630 | 635 | PF00069 | 0.428 |
MOD_OFUCOSY | 625 | 632 | PF10250 | 0.359 |
MOD_PIKK_1 | 200 | 206 | PF00454 | 0.373 |
MOD_PIKK_1 | 684 | 690 | PF00454 | 0.406 |
MOD_PIKK_1 | 87 | 93 | PF00454 | 0.359 |
MOD_PK_1 | 381 | 387 | PF00069 | 0.371 |
MOD_PK_1 | 682 | 688 | PF00069 | 0.248 |
MOD_PKA_1 | 381 | 387 | PF00069 | 0.468 |
MOD_PKA_2 | 381 | 387 | PF00069 | 0.501 |
MOD_Plk_1 | 150 | 156 | PF00069 | 0.406 |
MOD_Plk_1 | 159 | 165 | PF00069 | 0.525 |
MOD_Plk_1 | 269 | 275 | PF00069 | 0.389 |
MOD_Plk_1 | 366 | 372 | PF00069 | 0.489 |
MOD_Plk_1 | 619 | 625 | PF00069 | 0.461 |
MOD_Plk_2-3 | 24 | 30 | PF00069 | 0.406 |
MOD_Plk_2-3 | 489 | 495 | PF00069 | 0.367 |
MOD_Plk_2-3 | 608 | 614 | PF00069 | 0.543 |
MOD_Plk_4 | 104 | 110 | PF00069 | 0.343 |
MOD_Plk_4 | 13 | 19 | PF00069 | 0.413 |
MOD_Plk_4 | 140 | 146 | PF00069 | 0.431 |
MOD_Plk_4 | 150 | 156 | PF00069 | 0.355 |
MOD_Plk_4 | 195 | 201 | PF00069 | 0.389 |
MOD_Plk_4 | 40 | 46 | PF00069 | 0.389 |
MOD_Plk_4 | 465 | 471 | PF00069 | 0.435 |
MOD_Plk_4 | 598 | 604 | PF00069 | 0.415 |
MOD_ProDKin_1 | 402 | 408 | PF00069 | 0.667 |
MOD_ProDKin_1 | 422 | 428 | PF00069 | 0.415 |
MOD_ProDKin_1 | 69 | 75 | PF00069 | 0.389 |
MOD_SUMO_for_1 | 584 | 587 | PF00179 | 0.435 |
MOD_SUMO_rev_2 | 233 | 238 | PF00179 | 0.347 |
MOD_SUMO_rev_2 | 483 | 488 | PF00179 | 0.514 |
MOD_SUMO_rev_2 | 558 | 565 | PF00179 | 0.592 |
MOD_SUMO_rev_2 | 668 | 676 | PF00179 | 0.276 |
MOD_SUMO_rev_2 | 705 | 715 | PF00179 | 0.378 |
TRG_DiLeu_BaEn_4 | 547 | 553 | PF01217 | 0.527 |
TRG_ENDOCYTIC_2 | 171 | 174 | PF00928 | 0.389 |
TRG_ENDOCYTIC_2 | 231 | 234 | PF00928 | 0.389 |
TRG_ENDOCYTIC_2 | 535 | 538 | PF00928 | 0.518 |
TRG_ENDOCYTIC_2 | 626 | 629 | PF00928 | 0.426 |
TRG_ENDOCYTIC_2 | 667 | 670 | PF00928 | 0.406 |
TRG_ER_diArg_1 | 380 | 382 | PF00400 | 0.345 |
TRG_ER_diArg_1 | 569 | 572 | PF00400 | 0.554 |
TRG_ER_diArg_1 | 661 | 663 | PF00400 | 0.330 |
TRG_ER_FFAT_1 | 668 | 679 | PF00635 | 0.389 |
TRG_Pf-PMV_PEXEL_1 | 254 | 258 | PF00026 | 0.330 |
TRG_Pf-PMV_PEXEL_1 | 86 | 91 | PF00026 | 0.389 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6E2 | Leptomonas seymouri | 72% | 93% |
A0A0S4JRE7 | Bodo saltans | 41% | 100% |
A0A3S7X2D2 | Leishmania donovani | 86% | 99% |
A4I4I1 | Leishmania infantum | 86% | 99% |
E9ADY2 | Leishmania major | 85% | 100% |
E9ALU9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 99% |
Q875P5 | Lachancea kluyveri (strain ATCC 58438 / CBS 3082 / BCRC 21498 / NBRC 1685 / JCM 7257 / NCYC 543 / NRRL Y-12651) | 20% | 100% |