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. | yes | yes: 3 |
Pissara et al. | no | 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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0043226 | organelle | 2 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
Related structures:
AlphaFold database: E9ADY2
Term | Name | Level | Count |
---|---|---|---|
GO:0000413 | protein peptidyl-prolyl isomerization | 7 | 2 |
GO:0006457 | protein folding | 2 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0018193 | peptidyl-amino acid modification | 5 | 2 |
GO:0018208 | peptidyl-proline modification | 6 | 2 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0036211 | protein modification process | 4 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043412 | macromolecule modification | 4 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0061077 | chaperone-mediated protein folding | 3 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 9 |
GO:0003755 | peptidyl-prolyl cis-trans isomerase activity | 3 | 2 |
GO:0003824 | catalytic activity | 1 | 2 |
GO:0005488 | binding | 1 | 9 |
GO:0005524 | ATP binding | 5 | 9 |
GO:0016853 | isomerase activity | 2 | 2 |
GO:0016859 | cis-trans isomerase activity | 3 | 2 |
GO:0017076 | purine nucleotide binding | 4 | 9 |
GO:0030554 | adenyl nucleotide binding | 5 | 9 |
GO:0032553 | ribonucleotide binding | 3 | 9 |
GO:0032555 | purine ribonucleotide binding | 4 | 9 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 9 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 9 |
GO:0036094 | small molecule binding | 2 | 9 |
GO:0043167 | ion binding | 2 | 9 |
GO:0043168 | anion binding | 3 | 9 |
GO:0044183 | protein folding chaperone | 1 | 9 |
GO:0097159 | organic cyclic compound binding | 2 | 9 |
GO:0097367 | carbohydrate derivative binding | 2 | 9 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 2 |
GO:0140657 | ATP-dependent activity | 1 | 9 |
GO:0140662 | ATP-dependent protein folding chaperone | 2 | 9 |
GO:1901265 | nucleoside phosphate binding | 3 | 9 |
GO:1901363 | heterocyclic compound binding | 2 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 226 | 230 | PF00656 | 0.328 |
CLV_C14_Caspase3-7 | 421 | 425 | PF00656 | 0.604 |
CLV_C14_Caspase3-7 | 452 | 456 | PF00656 | 0.512 |
CLV_C14_Caspase3-7 | 497 | 501 | PF00656 | 0.390 |
CLV_NRD_NRD_1 | 258 | 260 | PF00675 | 0.382 |
CLV_NRD_NRD_1 | 265 | 267 | PF00675 | 0.338 |
CLV_NRD_NRD_1 | 545 | 547 | PF00675 | 0.490 |
CLV_NRD_NRD_1 | 578 | 580 | PF00675 | 0.465 |
CLV_NRD_NRD_1 | 664 | 666 | PF00675 | 0.343 |
CLV_PCSK_KEX2_1 | 545 | 547 | PF00082 | 0.506 |
CLV_PCSK_KEX2_1 | 577 | 579 | PF00082 | 0.513 |
CLV_PCSK_KEX2_1 | 620 | 622 | PF00082 | 0.474 |
CLV_PCSK_KEX2_1 | 664 | 666 | PF00082 | 0.377 |
CLV_PCSK_PC1ET2_1 | 545 | 547 | PF00082 | 0.506 |
CLV_PCSK_PC1ET2_1 | 577 | 579 | PF00082 | 0.565 |
CLV_PCSK_PC1ET2_1 | 620 | 622 | PF00082 | 0.473 |
CLV_PCSK_PC7_1 | 541 | 547 | PF00082 | 0.546 |
CLV_PCSK_PC7_1 | 573 | 579 | PF00082 | 0.548 |
CLV_PCSK_SKI1_1 | 112 | 116 | PF00082 | 0.336 |
CLV_PCSK_SKI1_1 | 12 | 16 | PF00082 | 0.418 |
CLV_PCSK_SKI1_1 | 146 | 150 | PF00082 | 0.454 |
CLV_PCSK_SKI1_1 | 259 | 263 | PF00082 | 0.384 |
CLV_PCSK_SKI1_1 | 266 | 270 | PF00082 | 0.347 |
CLV_PCSK_SKI1_1 | 312 | 316 | PF00082 | 0.366 |
CLV_PCSK_SKI1_1 | 358 | 362 | PF00082 | 0.330 |
CLV_PCSK_SKI1_1 | 387 | 391 | PF00082 | 0.522 |
CLV_PCSK_SKI1_1 | 41 | 45 | PF00082 | 0.359 |
CLV_PCSK_SKI1_1 | 439 | 443 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 660 | 664 | PF00082 | 0.340 |
CLV_PCSK_SKI1_1 | 703 | 707 | PF00082 | 0.507 |
CLV_PCSK_SKI1_1 | 714 | 718 | PF00082 | 0.503 |
DEG_APCC_DBOX_1 | 311 | 319 | PF00400 | 0.418 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.505 |
DEG_SPOP_SBC_1 | 271 | 275 | PF00917 | 0.424 |
DOC_ANK_TNKS_1 | 339 | 346 | PF00023 | 0.418 |
DOC_CYCLIN_yCln2_LP_2 | 100 | 106 | PF00134 | 0.400 |
DOC_MAPK_gen_1 | 545 | 554 | PF00069 | 0.524 |
DOC_MAPK_gen_1 | 617 | 625 | PF00069 | 0.464 |
DOC_MAPK_MEF2A_6 | 125 | 133 | PF00069 | 0.400 |
DOC_MAPK_MEF2A_6 | 68 | 76 | PF00069 | 0.400 |
DOC_PP2B_LxvP_1 | 131 | 134 | PF13499 | 0.418 |
DOC_PP2B_LxvP_1 | 322 | 325 | PF13499 | 0.304 |
DOC_USP7_MATH_1 | 132 | 136 | PF00917 | 0.393 |
DOC_USP7_MATH_1 | 323 | 327 | PF00917 | 0.257 |
DOC_USP7_MATH_1 | 377 | 381 | PF00917 | 0.418 |
DOC_USP7_MATH_1 | 483 | 487 | PF00917 | 0.643 |
DOC_USP7_MATH_1 | 632 | 636 | PF00917 | 0.450 |
DOC_USP7_UBL2_3 | 256 | 260 | PF12436 | 0.359 |
DOC_USP7_UBL2_3 | 710 | 714 | PF12436 | 0.477 |
DOC_USP7_UBL2_3 | 715 | 719 | PF12436 | 0.568 |
DOC_WW_Pin1_4 | 124 | 129 | PF00397 | 0.422 |
DOC_WW_Pin1_4 | 424 | 429 | PF00397 | 0.541 |
DOC_WW_Pin1_4 | 75 | 80 | PF00397 | 0.418 |
LIG_14-3-3_CanoR_1 | 146 | 151 | PF00244 | 0.328 |
LIG_14-3-3_CanoR_1 | 312 | 322 | PF00244 | 0.366 |
LIG_14-3-3_CanoR_1 | 365 | 371 | PF00244 | 0.351 |
LIG_14-3-3_CanoR_1 | 431 | 438 | PF00244 | 0.560 |
LIG_14-3-3_CanoR_1 | 439 | 447 | PF00244 | 0.620 |
LIG_Actin_WH2_2 | 209 | 224 | PF00022 | 0.418 |
LIG_Clathr_ClatBox_1 | 417 | 421 | PF01394 | 0.496 |
LIG_deltaCOP1_diTrp_1 | 588 | 598 | PF00928 | 0.471 |
LIG_EH1_1 | 108 | 116 | PF00400 | 0.396 |
LIG_FHA_1 | 124 | 130 | PF00498 | 0.446 |
LIG_FHA_1 | 18 | 24 | PF00498 | 0.420 |
LIG_FHA_1 | 440 | 446 | PF00498 | 0.453 |
LIG_FHA_1 | 594 | 600 | PF00498 | 0.428 |
LIG_FHA_1 | 647 | 653 | PF00498 | 0.479 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.473 |
LIG_FHA_2 | 272 | 278 | PF00498 | 0.378 |
LIG_FHA_2 | 47 | 53 | PF00498 | 0.362 |
LIG_FHA_2 | 59 | 65 | PF00498 | 0.364 |
LIG_FHA_2 | 609 | 615 | PF00498 | 0.517 |
LIG_FHA_2 | 678 | 684 | PF00498 | 0.267 |
LIG_Integrin_RGD_1 | 252 | 254 | PF01839 | 0.418 |
LIG_LIR_Gen_1 | 141 | 150 | PF02991 | 0.427 |
LIG_LIR_Gen_1 | 234 | 244 | PF02991 | 0.396 |
LIG_LIR_Gen_1 | 442 | 451 | PF02991 | 0.593 |
LIG_LIR_Gen_1 | 527 | 537 | PF02991 | 0.578 |
LIG_LIR_Gen_1 | 626 | 636 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 141 | 145 | PF02991 | 0.427 |
LIG_LIR_Nem_3 | 234 | 240 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 257 | 261 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 442 | 447 | PF02991 | 0.600 |
LIG_LIR_Nem_3 | 527 | 533 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 534 | 540 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 626 | 631 | PF02991 | 0.458 |
LIG_Pex14_1 | 56 | 60 | PF04695 | 0.418 |
LIG_Pex14_2 | 717 | 721 | PF04695 | 0.522 |
LIG_Rb_pABgroove_1 | 603 | 611 | PF01858 | 0.499 |
LIG_RPA_C_Fungi | 462 | 474 | PF08784 | 0.430 |
LIG_RPA_C_Fungi | 660 | 672 | PF08784 | 0.418 |
LIG_SH2_CRK | 177 | 181 | PF00017 | 0.418 |
LIG_SH2_CRK | 669 | 673 | PF00017 | 0.400 |
LIG_SH2_GRB2like | 628 | 631 | PF00017 | 0.456 |
LIG_SH2_SRC | 227 | 230 | PF00017 | 0.328 |
LIG_SH2_SRC | 628 | 631 | PF00017 | 0.456 |
LIG_SH2_SRC | 675 | 678 | PF00017 | 0.352 |
LIG_SH2_STAP1 | 138 | 142 | PF00017 | 0.256 |
LIG_SH2_STAP1 | 675 | 679 | PF00017 | 0.352 |
LIG_SH2_STAT3 | 471 | 474 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 110 | 113 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 171 | 174 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 227 | 230 | PF00017 | 0.378 |
LIG_SH2_STAT5 | 471 | 474 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 495 | 498 | PF00017 | 0.551 |
LIG_SH2_STAT5 | 502 | 505 | PF00017 | 0.581 |
LIG_SH2_STAT5 | 60 | 63 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 628 | 631 | PF00017 | 0.456 |
LIG_SH3_3 | 653 | 659 | PF00018 | 0.487 |
LIG_SH3_3 | 73 | 79 | PF00018 | 0.419 |
LIG_SUMO_SIM_anti_2 | 288 | 294 | PF11976 | 0.418 |
LIG_SUMO_SIM_par_1 | 189 | 195 | PF11976 | 0.356 |
LIG_SUMO_SIM_par_1 | 290 | 296 | PF11976 | 0.400 |
LIG_SUMO_SIM_par_1 | 691 | 698 | PF11976 | 0.368 |
LIG_TRAF2_1 | 612 | 615 | PF00917 | 0.592 |
LIG_TYR_ITIM | 175 | 180 | PF00017 | 0.400 |
LIG_UBA3_1 | 114 | 121 | PF00899 | 0.352 |
LIG_UBA3_1 | 314 | 321 | PF00899 | 0.412 |
LIG_WRC_WIRS_1 | 23 | 28 | PF05994 | 0.418 |
LIG_WRC_WIRS_1 | 255 | 260 | PF05994 | 0.418 |
LIG_WW_3 | 337 | 341 | PF00397 | 0.352 |
MOD_CDK_SPxxK_3 | 424 | 431 | PF00069 | 0.473 |
MOD_CK1_1 | 201 | 207 | PF00069 | 0.454 |
MOD_CK1_1 | 78 | 84 | PF00069 | 0.491 |
MOD_CK2_1 | 271 | 277 | PF00069 | 0.363 |
MOD_CK2_1 | 30 | 36 | PF00069 | 0.446 |
MOD_CK2_1 | 323 | 329 | PF00069 | 0.301 |
MOD_CK2_1 | 372 | 378 | PF00069 | 0.487 |
MOD_CK2_1 | 405 | 411 | PF00069 | 0.716 |
MOD_CK2_1 | 508 | 514 | PF00069 | 0.518 |
MOD_CK2_1 | 528 | 534 | PF00069 | 0.468 |
MOD_CK2_1 | 58 | 64 | PF00069 | 0.418 |
MOD_CK2_1 | 608 | 614 | PF00069 | 0.591 |
MOD_CK2_1 | 677 | 683 | PF00069 | 0.314 |
MOD_Cter_Amidation | 240 | 243 | PF01082 | 0.352 |
MOD_GlcNHglycan | 134 | 137 | PF01048 | 0.391 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.310 |
MOD_GlcNHglycan | 285 | 288 | PF01048 | 0.434 |
MOD_GlcNHglycan | 325 | 328 | PF01048 | 0.350 |
MOD_GlcNHglycan | 378 | 382 | PF01048 | 0.387 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.400 |
MOD_GlcNHglycan | 669 | 672 | PF01048 | 0.368 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.475 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.429 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.392 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.349 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.347 |
MOD_GSK3_1 | 397 | 404 | PF00069 | 0.739 |
MOD_GSK3_1 | 483 | 490 | PF00069 | 0.485 |
MOD_GSK3_1 | 524 | 531 | PF00069 | 0.595 |
MOD_GSK3_1 | 560 | 567 | PF00069 | 0.702 |
MOD_N-GLC_1 | 372 | 377 | PF02516 | 0.400 |
MOD_N-GLC_1 | 615 | 620 | PF02516 | 0.539 |
MOD_N-GLC_1 | 646 | 651 | PF02516 | 0.499 |
MOD_N-GLC_2 | 646 | 648 | PF02516 | 0.498 |
MOD_NEK2_1 | 123 | 128 | PF00069 | 0.414 |
MOD_NEK2_1 | 175 | 180 | PF00069 | 0.335 |
MOD_NEK2_1 | 231 | 236 | PF00069 | 0.418 |
MOD_NEK2_1 | 361 | 366 | PF00069 | 0.371 |
MOD_NEK2_1 | 58 | 63 | PF00069 | 0.418 |
MOD_NEK2_1 | 608 | 613 | PF00069 | 0.555 |
MOD_NEK2_2 | 536 | 541 | PF00069 | 0.529 |
MOD_NEK2_2 | 632 | 637 | PF00069 | 0.462 |
MOD_OFUCOSY | 627 | 634 | PF10250 | 0.391 |
MOD_PIKK_1 | 206 | 212 | PF00454 | 0.407 |
MOD_PIKK_1 | 275 | 281 | PF00454 | 0.352 |
MOD_PIKK_1 | 329 | 335 | PF00454 | 0.352 |
MOD_PIKK_1 | 686 | 692 | PF00454 | 0.608 |
MOD_Plk_1 | 156 | 162 | PF00069 | 0.403 |
MOD_Plk_1 | 165 | 171 | PF00069 | 0.338 |
MOD_Plk_1 | 275 | 281 | PF00069 | 0.418 |
MOD_Plk_1 | 372 | 378 | PF00069 | 0.502 |
MOD_Plk_1 | 508 | 514 | PF00069 | 0.409 |
MOD_Plk_1 | 621 | 627 | PF00069 | 0.492 |
MOD_Plk_2-3 | 30 | 36 | PF00069 | 0.400 |
MOD_Plk_2-3 | 509 | 515 | PF00069 | 0.376 |
MOD_Plk_2-3 | 528 | 534 | PF00069 | 0.532 |
MOD_Plk_2-3 | 610 | 616 | PF00069 | 0.552 |
MOD_Plk_2-3 | 677 | 683 | PF00069 | 0.267 |
MOD_Plk_4 | 110 | 116 | PF00069 | 0.400 |
MOD_Plk_4 | 146 | 152 | PF00069 | 0.480 |
MOD_Plk_4 | 156 | 162 | PF00069 | 0.429 |
MOD_Plk_4 | 19 | 25 | PF00069 | 0.444 |
MOD_Plk_4 | 201 | 207 | PF00069 | 0.363 |
MOD_Plk_4 | 46 | 52 | PF00069 | 0.418 |
MOD_Plk_4 | 467 | 473 | PF00069 | 0.428 |
MOD_Plk_4 | 6 | 12 | PF00069 | 0.411 |
MOD_Plk_4 | 600 | 606 | PF00069 | 0.456 |
MOD_ProDKin_1 | 124 | 130 | PF00069 | 0.422 |
MOD_ProDKin_1 | 424 | 430 | PF00069 | 0.534 |
MOD_ProDKin_1 | 75 | 81 | PF00069 | 0.418 |
MOD_SUMO_rev_2 | 249 | 258 | PF00179 | 0.461 |
MOD_SUMO_rev_2 | 485 | 490 | PF00179 | 0.513 |
MOD_SUMO_rev_2 | 560 | 567 | PF00179 | 0.632 |
MOD_SUMO_rev_2 | 610 | 618 | PF00179 | 0.526 |
TRG_DiLeu_BaEn_4 | 549 | 555 | PF01217 | 0.563 |
TRG_ENDOCYTIC_2 | 177 | 180 | PF00928 | 0.418 |
TRG_ENDOCYTIC_2 | 237 | 240 | PF00928 | 0.418 |
TRG_ENDOCYTIC_2 | 537 | 540 | PF00928 | 0.566 |
TRG_ENDOCYTIC_2 | 628 | 631 | PF00928 | 0.456 |
TRG_ENDOCYTIC_2 | 669 | 672 | PF00928 | 0.400 |
TRG_ER_diArg_1 | 571 | 574 | PF00400 | 0.567 |
TRG_ER_diArg_1 | 663 | 665 | PF00400 | 0.377 |
TRG_ER_FFAT_1 | 670 | 681 | PF00635 | 0.418 |
TRG_Pf-PMV_PEXEL_1 | 260 | 264 | PF00026 | 0.359 |
TRG_Pf-PMV_PEXEL_1 | 431 | 435 | PF00026 | 0.481 |
TRG_Pf-PMV_PEXEL_1 | 92 | 97 | PF00026 | 0.418 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6E2 | Leptomonas seymouri | 71% | 93% |
A0A0S4JRE7 | Bodo saltans | 41% | 100% |
A0A3S7X2D2 | Leishmania donovani | 94% | 100% |
A4HHD6 | Leishmania braziliensis | 85% | 100% |
A4I4I1 | Leishmania infantum | 94% | 100% |
E9ALU9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
V5BI61 | Trypanosoma cruzi | 24% | 100% |