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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
GO:0005783 | endoplasmic reticulum | 5 | 1 |
GO:0005794 | Golgi apparatus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
Related structures:
AlphaFold database: E9AWG4
Term | Name | Level | Count |
---|---|---|---|
GO:0006497 | protein lipidation | 5 | 1 |
GO:0006605 | protein targeting | 5 | 1 |
GO:0006612 | protein targeting to membrane | 5 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0006810 | transport | 3 | 1 |
GO:0006886 | intracellular protein transport | 4 | 1 |
GO:0008104 | protein localization | 4 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0015031 | protein transport | 4 | 1 |
GO:0018193 | peptidyl-amino acid modification | 5 | 1 |
GO:0018198 | peptidyl-cysteine modification | 6 | 1 |
GO:0018230 | peptidyl-L-cysteine S-palmitoylation | 7 | 1 |
GO:0018231 | peptidyl-S-diacylglycerol-L-cysteine biosynthetic process from peptidyl-cysteine | 7 | 1 |
GO:0018345 | protein palmitoylation | 6 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0033036 | macromolecule localization | 2 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0043543 | protein acylation | 5 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0045184 | establishment of protein localization | 3 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
GO:0051668 | localization within membrane | 3 | 1 |
GO:0070727 | cellular macromolecule localization | 3 | 1 |
GO:0071702 | organic substance transport | 4 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0071705 | nitrogen compound transport | 4 | 1 |
GO:0072657 | protein localization to membrane | 4 | 1 |
GO:0090150 | establishment of protein localization to membrane | 4 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0016409 | palmitoyltransferase activity | 5 | 7 |
GO:0016417 | S-acyltransferase activity | 5 | 7 |
GO:0016740 | transferase activity | 2 | 7 |
GO:0016746 | acyltransferase activity | 3 | 7 |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 7 |
GO:0019706 | protein-cysteine S-palmitoyltransferase activity | 4 | 7 |
GO:0019707 | protein-cysteine S-acyltransferase activity | 3 | 7 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 213 | 217 | PF00656 | 0.675 |
CLV_NRD_NRD_1 | 130 | 132 | PF00675 | 0.404 |
CLV_NRD_NRD_1 | 363 | 365 | PF00675 | 0.483 |
CLV_NRD_NRD_1 | 565 | 567 | PF00675 | 0.441 |
CLV_NRD_NRD_1 | 597 | 599 | PF00675 | 0.440 |
CLV_PCSK_KEX2_1 | 130 | 132 | PF00082 | 0.401 |
CLV_PCSK_KEX2_1 | 363 | 365 | PF00082 | 0.483 |
CLV_PCSK_KEX2_1 | 565 | 567 | PF00082 | 0.441 |
CLV_PCSK_KEX2_1 | 597 | 599 | PF00082 | 0.433 |
CLV_PCSK_SKI1_1 | 106 | 110 | PF00082 | 0.317 |
CLV_PCSK_SKI1_1 | 412 | 416 | PF00082 | 0.255 |
CLV_PCSK_SKI1_1 | 434 | 438 | PF00082 | 0.276 |
CLV_PCSK_SKI1_1 | 74 | 78 | PF00082 | 0.536 |
DEG_APCC_DBOX_1 | 609 | 617 | PF00400 | 0.708 |
DEG_SCF_FBW7_1 | 242 | 249 | PF00400 | 0.608 |
DEG_SPOP_SBC_1 | 306 | 310 | PF00917 | 0.638 |
DOC_CKS1_1 | 121 | 126 | PF01111 | 0.561 |
DOC_MAPK_gen_1 | 130 | 136 | PF00069 | 0.640 |
DOC_MAPK_gen_1 | 363 | 371 | PF00069 | 0.577 |
DOC_MAPK_gen_1 | 597 | 606 | PF00069 | 0.602 |
DOC_MAPK_MEF2A_6 | 26 | 33 | PF00069 | 0.390 |
DOC_MAPK_MEF2A_6 | 373 | 382 | PF00069 | 0.628 |
DOC_PP1_RVXF_1 | 104 | 110 | PF00149 | 0.570 |
DOC_PP1_RVXF_1 | 133 | 139 | PF00149 | 0.640 |
DOC_PP2B_LxvP_1 | 619 | 622 | PF13499 | 0.666 |
DOC_PP4_FxxP_1 | 109 | 112 | PF00568 | 0.634 |
DOC_PP4_FxxP_1 | 206 | 209 | PF00568 | 0.711 |
DOC_PP4_FxxP_1 | 606 | 609 | PF00568 | 0.617 |
DOC_SPAK_OSR1_1 | 601 | 605 | PF12202 | 0.508 |
DOC_USP7_MATH_1 | 196 | 200 | PF00917 | 0.723 |
DOC_USP7_MATH_1 | 212 | 216 | PF00917 | 0.670 |
DOC_USP7_MATH_1 | 236 | 240 | PF00917 | 0.774 |
DOC_USP7_MATH_1 | 289 | 293 | PF00917 | 0.645 |
DOC_USP7_MATH_1 | 313 | 317 | PF00917 | 0.701 |
DOC_USP7_MATH_1 | 324 | 328 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 330 | 334 | PF00917 | 0.628 |
DOC_USP7_MATH_1 | 386 | 390 | PF00917 | 0.569 |
DOC_USP7_MATH_1 | 401 | 405 | PF00917 | 0.476 |
DOC_USP7_MATH_1 | 448 | 452 | PF00917 | 0.351 |
DOC_USP7_MATH_1 | 622 | 626 | PF00917 | 0.721 |
DOC_USP7_MATH_2 | 63 | 69 | PF00917 | 0.425 |
DOC_WW_Pin1_4 | 120 | 125 | PF00397 | 0.660 |
DOC_WW_Pin1_4 | 192 | 197 | PF00397 | 0.779 |
DOC_WW_Pin1_4 | 199 | 204 | PF00397 | 0.710 |
DOC_WW_Pin1_4 | 221 | 226 | PF00397 | 0.759 |
DOC_WW_Pin1_4 | 227 | 232 | PF00397 | 0.741 |
DOC_WW_Pin1_4 | 242 | 247 | PF00397 | 0.692 |
DOC_WW_Pin1_4 | 292 | 297 | PF00397 | 0.780 |
DOC_WW_Pin1_4 | 326 | 331 | PF00397 | 0.832 |
DOC_WW_Pin1_4 | 617 | 622 | PF00397 | 0.721 |
LIG_14-3-3_CanoR_1 | 106 | 112 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 11 | 16 | PF00244 | 0.646 |
LIG_14-3-3_CanoR_1 | 363 | 372 | PF00244 | 0.622 |
LIG_14-3-3_CanoR_1 | 498 | 504 | PF00244 | 0.491 |
LIG_14-3-3_CanoR_1 | 566 | 575 | PF00244 | 0.652 |
LIG_14-3-3_CanoR_1 | 629 | 637 | PF00244 | 0.639 |
LIG_BIR_III_2 | 353 | 357 | PF00653 | 0.714 |
LIG_BRCT_BRCA1_1 | 388 | 392 | PF00533 | 0.476 |
LIG_BRCT_BRCA1_1 | 450 | 454 | PF00533 | 0.297 |
LIG_BRCT_BRCA1_1 | 510 | 514 | PF00533 | 0.575 |
LIG_Clathr_ClatBox_1 | 254 | 258 | PF01394 | 0.603 |
LIG_CSL_BTD_1 | 472 | 475 | PF09270 | 0.276 |
LIG_deltaCOP1_diTrp_1 | 118 | 126 | PF00928 | 0.606 |
LIG_deltaCOP1_diTrp_1 | 466 | 473 | PF00928 | 0.276 |
LIG_eIF4E_1 | 25 | 31 | PF01652 | 0.237 |
LIG_FHA_1 | 243 | 249 | PF00498 | 0.681 |
LIG_FHA_1 | 326 | 332 | PF00498 | 0.671 |
LIG_FHA_1 | 338 | 344 | PF00498 | 0.628 |
LIG_FHA_1 | 34 | 40 | PF00498 | 0.426 |
LIG_FHA_1 | 450 | 456 | PF00498 | 0.341 |
LIG_FHA_1 | 56 | 62 | PF00498 | 0.423 |
LIG_FHA_1 | 85 | 91 | PF00498 | 0.378 |
LIG_FHA_2 | 348 | 354 | PF00498 | 0.808 |
LIG_Integrin_RGD_1 | 580 | 582 | PF01839 | 0.531 |
LIG_LIR_Apic_2 | 5 | 10 | PF02991 | 0.557 |
LIG_LIR_Gen_1 | 103 | 112 | PF02991 | 0.563 |
LIG_LIR_Gen_1 | 451 | 462 | PF02991 | 0.351 |
LIG_LIR_Nem_3 | 103 | 107 | PF02991 | 0.556 |
LIG_LIR_Nem_3 | 14 | 18 | PF02991 | 0.628 |
LIG_LIR_Nem_3 | 389 | 395 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 451 | 457 | PF02991 | 0.351 |
LIG_NRBOX | 553 | 559 | PF00104 | 0.539 |
LIG_Pex14_2 | 437 | 441 | PF04695 | 0.313 |
LIG_Pex14_2 | 602 | 606 | PF04695 | 0.617 |
LIG_PTAP_UEV_1 | 587 | 592 | PF05743 | 0.725 |
LIG_REV1ctd_RIR_1 | 43 | 52 | PF16727 | 0.318 |
LIG_SH2_CRK | 180 | 184 | PF00017 | 0.596 |
LIG_SH2_CRK | 25 | 29 | PF00017 | 0.417 |
LIG_SH2_CRK | 442 | 446 | PF00017 | 0.340 |
LIG_SH2_CRK | 614 | 618 | PF00017 | 0.792 |
LIG_SH2_CRK | 7 | 11 | PF00017 | 0.555 |
LIG_SH2_SRC | 114 | 117 | PF00017 | 0.543 |
LIG_SH2_SRC | 180 | 183 | PF00017 | 0.596 |
LIG_SH2_SRC | 479 | 482 | PF00017 | 0.209 |
LIG_SH2_STAT5 | 101 | 104 | PF00017 | 0.372 |
LIG_SH2_STAT5 | 114 | 117 | PF00017 | 0.539 |
LIG_SH2_STAT5 | 122 | 125 | PF00017 | 0.638 |
LIG_SH2_STAT5 | 435 | 438 | PF00017 | 0.390 |
LIG_SH2_STAT5 | 487 | 490 | PF00017 | 0.351 |
LIG_SH2_STAT5 | 75 | 78 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 79 | 82 | PF00017 | 0.373 |
LIG_SH3_3 | 113 | 119 | PF00018 | 0.687 |
LIG_SH3_3 | 222 | 228 | PF00018 | 0.712 |
LIG_SH3_3 | 523 | 529 | PF00018 | 0.663 |
LIG_SH3_3 | 585 | 591 | PF00018 | 0.756 |
LIG_SH3_3 | 615 | 621 | PF00018 | 0.667 |
LIG_SUMO_SIM_anti_2 | 367 | 375 | PF11976 | 0.568 |
LIG_TRAF2_1 | 159 | 162 | PF00917 | 0.609 |
LIG_TRFH_1 | 614 | 618 | PF08558 | 0.717 |
LIG_TYR_ITIM | 440 | 445 | PF00017 | 0.340 |
LIG_TYR_ITIM | 485 | 490 | PF00017 | 0.351 |
LIG_WRC_WIRS_1 | 101 | 106 | PF05994 | 0.335 |
LIG_WW_1 | 177 | 180 | PF00397 | 0.561 |
MOD_CDK_SPK_2 | 120 | 125 | PF00069 | 0.659 |
MOD_CDK_SPxK_1 | 331 | 337 | PF00069 | 0.741 |
MOD_CK1_1 | 199 | 205 | PF00069 | 0.710 |
MOD_CK1_1 | 253 | 259 | PF00069 | 0.603 |
MOD_CK1_1 | 292 | 298 | PF00069 | 0.712 |
MOD_CK1_1 | 315 | 321 | PF00069 | 0.698 |
MOD_CK1_1 | 325 | 331 | PF00069 | 0.674 |
MOD_CK1_1 | 521 | 527 | PF00069 | 0.671 |
MOD_CK1_1 | 531 | 537 | PF00069 | 0.665 |
MOD_CK1_1 | 573 | 579 | PF00069 | 0.738 |
MOD_CK1_1 | 589 | 595 | PF00069 | 0.752 |
MOD_CK2_1 | 498 | 504 | PF00069 | 0.495 |
MOD_CK2_1 | 514 | 520 | PF00069 | 0.631 |
MOD_GlcNHglycan | 138 | 141 | PF01048 | 0.442 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.481 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.462 |
MOD_GlcNHglycan | 242 | 245 | PF01048 | 0.414 |
MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.561 |
MOD_GlcNHglycan | 285 | 288 | PF01048 | 0.456 |
MOD_GlcNHglycan | 291 | 294 | PF01048 | 0.416 |
MOD_GlcNHglycan | 322 | 325 | PF01048 | 0.528 |
MOD_GlcNHglycan | 33 | 36 | PF01048 | 0.313 |
MOD_GlcNHglycan | 481 | 484 | PF01048 | 0.286 |
MOD_GlcNHglycan | 520 | 523 | PF01048 | 0.458 |
MOD_GlcNHglycan | 577 | 580 | PF01048 | 0.500 |
MOD_GlcNHglycan | 588 | 591 | PF01048 | 0.481 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.348 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.725 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.690 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.688 |
MOD_GSK3_1 | 236 | 243 | PF00069 | 0.778 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.647 |
MOD_GSK3_1 | 279 | 286 | PF00069 | 0.688 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.690 |
MOD_GSK3_1 | 301 | 308 | PF00069 | 0.791 |
MOD_GSK3_1 | 309 | 316 | PF00069 | 0.802 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.636 |
MOD_GSK3_1 | 326 | 333 | PF00069 | 0.659 |
MOD_GSK3_1 | 449 | 456 | PF00069 | 0.395 |
MOD_GSK3_1 | 504 | 511 | PF00069 | 0.639 |
MOD_GSK3_1 | 514 | 521 | PF00069 | 0.641 |
MOD_GSK3_1 | 567 | 574 | PF00069 | 0.706 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.317 |
MOD_LATS_1 | 362 | 368 | PF00433 | 0.682 |
MOD_N-GLC_1 | 449 | 454 | PF02516 | 0.325 |
MOD_NEK2_1 | 100 | 105 | PF00069 | 0.380 |
MOD_NEK2_1 | 134 | 139 | PF00069 | 0.667 |
MOD_NEK2_1 | 322 | 327 | PF00069 | 0.640 |
MOD_NEK2_1 | 441 | 446 | PF00069 | 0.350 |
MOD_NEK2_1 | 453 | 458 | PF00069 | 0.349 |
MOD_NEK2_1 | 514 | 519 | PF00069 | 0.604 |
MOD_NEK2_1 | 567 | 572 | PF00069 | 0.655 |
MOD_NEK2_1 | 575 | 580 | PF00069 | 0.806 |
MOD_NEK2_1 | 77 | 82 | PF00069 | 0.342 |
MOD_NEK2_2 | 357 | 362 | PF00069 | 0.632 |
MOD_NEK2_2 | 386 | 391 | PF00069 | 0.568 |
MOD_PIKK_1 | 521 | 527 | PF00454 | 0.671 |
MOD_PKA_2 | 336 | 342 | PF00069 | 0.723 |
MOD_PKA_2 | 504 | 510 | PF00069 | 0.579 |
MOD_PKB_1 | 627 | 635 | PF00069 | 0.639 |
MOD_Plk_1 | 449 | 455 | PF00069 | 0.325 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.568 |
MOD_Plk_4 | 214 | 220 | PF00069 | 0.806 |
MOD_Plk_4 | 250 | 256 | PF00069 | 0.608 |
MOD_Plk_4 | 449 | 455 | PF00069 | 0.474 |
MOD_ProDKin_1 | 120 | 126 | PF00069 | 0.658 |
MOD_ProDKin_1 | 192 | 198 | PF00069 | 0.775 |
MOD_ProDKin_1 | 199 | 205 | PF00069 | 0.712 |
MOD_ProDKin_1 | 221 | 227 | PF00069 | 0.759 |
MOD_ProDKin_1 | 242 | 248 | PF00069 | 0.727 |
MOD_ProDKin_1 | 292 | 298 | PF00069 | 0.781 |
MOD_ProDKin_1 | 326 | 332 | PF00069 | 0.831 |
MOD_ProDKin_1 | 617 | 623 | PF00069 | 0.724 |
TRG_DiLeu_BaLyEn_6 | 25 | 30 | PF01217 | 0.390 |
TRG_DiLeu_BaLyEn_6 | 45 | 50 | PF01217 | 0.295 |
TRG_ENDOCYTIC_2 | 101 | 104 | PF00928 | 0.530 |
TRG_ENDOCYTIC_2 | 42 | 45 | PF00928 | 0.273 |
TRG_ENDOCYTIC_2 | 433 | 436 | PF00928 | 0.503 |
TRG_ENDOCYTIC_2 | 442 | 445 | PF00928 | 0.351 |
TRG_ENDOCYTIC_2 | 487 | 490 | PF00928 | 0.351 |
TRG_ENDOCYTIC_2 | 614 | 617 | PF00928 | 0.793 |
TRG_ER_diArg_1 | 10 | 13 | PF00400 | 0.604 |
TRG_ER_diArg_1 | 363 | 365 | PF00400 | 0.683 |
TRG_ER_diArg_1 | 564 | 566 | PF00400 | 0.688 |
TRG_ER_diArg_1 | 608 | 611 | PF00400 | 0.650 |
TRG_ER_diArg_1 | 628 | 631 | PF00400 | 0.702 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P628 | Leptomonas seymouri | 36% | 98% |
A0A3S7WXW1 | Leishmania donovani | 84% | 100% |
A4HD17 | Leishmania braziliensis | 60% | 100% |
A4I0K3 | Leishmania infantum | 84% | 100% |
Q4QB07 | Leishmania major | 82% | 100% |