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: A4HD17
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 | 344 | 348 | PF00656 | 0.631 |
CLV_C14_Caspase3-7 | 573 | 577 | PF00656 | 0.604 |
CLV_NRD_NRD_1 | 516 | 518 | PF00675 | 0.386 |
CLV_NRD_NRD_1 | 559 | 561 | PF00675 | 0.456 |
CLV_NRD_NRD_1 | 591 | 593 | PF00675 | 0.418 |
CLV_PCSK_FUR_1 | 588 | 592 | PF00082 | 0.368 |
CLV_PCSK_KEX2_1 | 516 | 518 | PF00082 | 0.411 |
CLV_PCSK_KEX2_1 | 559 | 561 | PF00082 | 0.456 |
CLV_PCSK_KEX2_1 | 590 | 592 | PF00082 | 0.411 |
CLV_PCSK_PC1ET2_1 | 590 | 592 | PF00082 | 0.331 |
CLV_PCSK_SKI1_1 | 106 | 110 | PF00082 | 0.311 |
CLV_PCSK_SKI1_1 | 240 | 244 | PF00082 | 0.414 |
CLV_PCSK_SKI1_1 | 406 | 410 | PF00082 | 0.255 |
CLV_PCSK_SKI1_1 | 428 | 432 | PF00082 | 0.276 |
CLV_PCSK_SKI1_1 | 595 | 599 | PF00082 | 0.404 |
CLV_PCSK_SKI1_1 | 604 | 608 | PF00082 | 0.378 |
CLV_PCSK_SKI1_1 | 74 | 78 | PF00082 | 0.544 |
DEG_APCC_DBOX_1 | 603 | 611 | PF00400 | 0.641 |
DEG_SCF_FBW7_2 | 326 | 332 | PF00400 | 0.613 |
DEG_SPOP_SBC_1 | 288 | 292 | PF00917 | 0.750 |
DEG_SPOP_SBC_1 | 298 | 302 | PF00917 | 0.686 |
DOC_CKS1_1 | 326 | 331 | PF01111 | 0.614 |
DOC_CKS1_1 | 359 | 364 | PF01111 | 0.616 |
DOC_CYCLIN_RxL_1 | 129 | 137 | PF00134 | 0.533 |
DOC_CYCLIN_yCln2_LP_2 | 359 | 365 | PF00134 | 0.614 |
DOC_MAPK_gen_1 | 590 | 600 | PF00069 | 0.584 |
DOC_MAPK_MEF2A_6 | 26 | 33 | PF00069 | 0.390 |
DOC_PP1_RVXF_1 | 104 | 110 | PF00149 | 0.566 |
DOC_PP4_FxxP_1 | 285 | 288 | PF00568 | 0.647 |
DOC_PP4_FxxP_1 | 600 | 603 | PF00568 | 0.587 |
DOC_USP7_MATH_1 | 236 | 240 | PF00917 | 0.765 |
DOC_USP7_MATH_1 | 250 | 254 | PF00917 | 0.600 |
DOC_USP7_MATH_1 | 288 | 292 | PF00917 | 0.664 |
DOC_USP7_MATH_1 | 293 | 297 | PF00917 | 0.655 |
DOC_USP7_MATH_1 | 305 | 309 | PF00917 | 0.687 |
DOC_USP7_MATH_1 | 318 | 322 | PF00917 | 0.673 |
DOC_USP7_MATH_1 | 350 | 354 | PF00917 | 0.651 |
DOC_USP7_MATH_1 | 365 | 369 | PF00917 | 0.656 |
DOC_USP7_MATH_1 | 380 | 384 | PF00917 | 0.551 |
DOC_USP7_MATH_1 | 395 | 399 | PF00917 | 0.476 |
DOC_USP7_MATH_1 | 510 | 514 | PF00917 | 0.558 |
DOC_WW_Pin1_4 | 192 | 197 | PF00397 | 0.781 |
DOC_WW_Pin1_4 | 227 | 232 | PF00397 | 0.734 |
DOC_WW_Pin1_4 | 289 | 294 | PF00397 | 0.775 |
DOC_WW_Pin1_4 | 320 | 325 | PF00397 | 0.822 |
DOC_WW_Pin1_4 | 339 | 344 | PF00397 | 0.613 |
DOC_WW_Pin1_4 | 358 | 363 | PF00397 | 0.654 |
DOC_WW_Pin1_4 | 515 | 520 | PF00397 | 0.583 |
DOC_WW_Pin1_4 | 611 | 616 | PF00397 | 0.628 |
LIG_14-3-3_CanoR_1 | 106 | 116 | PF00244 | 0.512 |
LIG_14-3-3_CanoR_1 | 11 | 16 | PF00244 | 0.635 |
LIG_14-3-3_CanoR_1 | 492 | 498 | PF00244 | 0.489 |
LIG_14-3-3_CanoR_1 | 592 | 600 | PF00244 | 0.684 |
LIG_Actin_WH2_2 | 465 | 480 | PF00022 | 0.211 |
LIG_Actin_WH2_2 | 92 | 108 | PF00022 | 0.219 |
LIG_BIR_III_2 | 347 | 351 | PF00653 | 0.750 |
LIG_BRCT_BRCA1_1 | 33 | 37 | PF00533 | 0.228 |
LIG_BRCT_BRCA1_1 | 382 | 386 | PF00533 | 0.476 |
LIG_CSL_BTD_1 | 181 | 184 | PF09270 | 0.558 |
LIG_CSL_BTD_1 | 466 | 469 | PF09270 | 0.276 |
LIG_deltaCOP1_diTrp_1 | 460 | 467 | PF00928 | 0.276 |
LIG_deltaCOP1_diTrp_1 | 481 | 488 | PF00928 | 0.222 |
LIG_eIF4E_1 | 25 | 31 | PF01652 | 0.237 |
LIG_EVH1_2 | 225 | 229 | PF00568 | 0.621 |
LIG_FHA_1 | 243 | 249 | PF00498 | 0.678 |
LIG_FHA_1 | 299 | 305 | PF00498 | 0.650 |
LIG_FHA_1 | 321 | 327 | PF00498 | 0.670 |
LIG_FHA_1 | 34 | 40 | PF00498 | 0.419 |
LIG_FHA_1 | 444 | 450 | PF00498 | 0.338 |
LIG_FHA_1 | 56 | 62 | PF00498 | 0.434 |
LIG_FHA_1 | 564 | 570 | PF00498 | 0.618 |
LIG_FHA_1 | 594 | 600 | PF00498 | 0.505 |
LIG_FHA_2 | 124 | 130 | PF00498 | 0.544 |
LIG_FHA_2 | 342 | 348 | PF00498 | 0.831 |
LIG_FHA_2 | 67 | 73 | PF00498 | 0.349 |
LIG_LIR_Apic_2 | 283 | 288 | PF02991 | 0.645 |
LIG_LIR_Apic_2 | 464 | 469 | PF02991 | 0.211 |
LIG_LIR_Gen_1 | 103 | 112 | PF02991 | 0.557 |
LIG_LIR_Gen_1 | 383 | 393 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 103 | 107 | PF02991 | 0.553 |
LIG_LIR_Nem_3 | 14 | 18 | PF02991 | 0.609 |
LIG_LIR_Nem_3 | 383 | 389 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 464 | 468 | PF02991 | 0.211 |
LIG_LIR_Nem_3 | 535 | 541 | PF02991 | 0.537 |
LIG_Pex14_2 | 431 | 435 | PF04695 | 0.313 |
LIG_REV1ctd_RIR_1 | 43 | 52 | PF16727 | 0.317 |
LIG_SH2_CRK | 25 | 29 | PF00017 | 0.430 |
LIG_SH2_CRK | 538 | 542 | PF00017 | 0.529 |
LIG_SH2_CRK | 608 | 612 | PF00017 | 0.686 |
LIG_SH2_SRC | 114 | 117 | PF00017 | 0.534 |
LIG_SH2_STAT5 | 114 | 117 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 429 | 432 | PF00017 | 0.390 |
LIG_SH2_STAT5 | 452 | 455 | PF00017 | 0.208 |
LIG_SH2_STAT5 | 538 | 541 | PF00017 | 0.535 |
LIG_SH2_STAT5 | 75 | 78 | PF00017 | 0.423 |
LIG_SH3_2 | 116 | 121 | PF14604 | 0.612 |
LIG_SH3_3 | 113 | 119 | PF00018 | 0.685 |
LIG_SH3_3 | 181 | 187 | PF00018 | 0.631 |
LIG_SH3_3 | 220 | 226 | PF00018 | 0.710 |
LIG_SH3_3 | 323 | 329 | PF00018 | 0.640 |
LIG_SH3_3 | 509 | 515 | PF00018 | 0.629 |
LIG_SH3_3 | 576 | 582 | PF00018 | 0.698 |
LIG_SH3_3 | 609 | 615 | PF00018 | 0.563 |
LIG_SUMO_SIM_anti_2 | 58 | 65 | PF11976 | 0.340 |
LIG_SUMO_SIM_par_1 | 58 | 65 | PF11976 | 0.340 |
LIG_SUMO_SIM_par_1 | 580 | 586 | PF11976 | 0.584 |
LIG_TRAF2_1 | 69 | 72 | PF00917 | 0.351 |
LIG_TRFH_1 | 608 | 612 | PF08558 | 0.611 |
LIG_WRC_WIRS_1 | 101 | 106 | PF05994 | 0.333 |
MOD_CDK_SPK_2 | 227 | 232 | PF00069 | 0.629 |
MOD_CK1_1 | 192 | 198 | PF00069 | 0.713 |
MOD_CK1_1 | 199 | 205 | PF00069 | 0.709 |
MOD_CK1_1 | 214 | 220 | PF00069 | 0.694 |
MOD_CK1_1 | 230 | 236 | PF00069 | 0.666 |
MOD_CK1_1 | 283 | 289 | PF00069 | 0.692 |
MOD_CK1_1 | 291 | 297 | PF00069 | 0.731 |
MOD_CK1_1 | 309 | 315 | PF00069 | 0.695 |
MOD_CK1_1 | 316 | 322 | PF00069 | 0.670 |
MOD_CK1_1 | 525 | 531 | PF00069 | 0.691 |
MOD_CK1_1 | 555 | 561 | PF00069 | 0.620 |
MOD_CK1_1 | 567 | 573 | PF00069 | 0.747 |
MOD_CK2_1 | 123 | 129 | PF00069 | 0.549 |
MOD_CK2_1 | 182 | 188 | PF00069 | 0.574 |
MOD_CK2_1 | 291 | 297 | PF00069 | 0.736 |
MOD_CK2_1 | 525 | 531 | PF00069 | 0.580 |
MOD_CK2_1 | 66 | 72 | PF00069 | 0.377 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.469 |
MOD_GlcNHglycan | 259 | 262 | PF01048 | 0.443 |
MOD_GlcNHglycan | 272 | 275 | PF01048 | 0.567 |
MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.521 |
MOD_GlcNHglycan | 33 | 36 | PF01048 | 0.313 |
MOD_GlcNHglycan | 336 | 339 | PF01048 | 0.404 |
MOD_GlcNHglycan | 454 | 457 | PF01048 | 0.432 |
MOD_GlcNHglycan | 502 | 506 | PF01048 | 0.330 |
MOD_GlcNHglycan | 512 | 515 | PF01048 | 0.450 |
MOD_GlcNHglycan | 570 | 573 | PF01048 | 0.495 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.719 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.657 |
MOD_GSK3_1 | 214 | 221 | PF00069 | 0.680 |
MOD_GSK3_1 | 283 | 290 | PF00069 | 0.707 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.709 |
MOD_GSK3_1 | 303 | 310 | PF00069 | 0.796 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.630 |
MOD_GSK3_1 | 443 | 450 | PF00069 | 0.395 |
MOD_GSK3_1 | 515 | 522 | PF00069 | 0.609 |
MOD_GSK3_1 | 561 | 568 | PF00069 | 0.725 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.464 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.324 |
MOD_N-GLC_1 | 443 | 448 | PF02516 | 0.325 |
MOD_N-GLC_1 | 56 | 61 | PF02516 | 0.509 |
MOD_N-GLC_2 | 419 | 421 | PF02516 | 0.298 |
MOD_NEK2_1 | 100 | 105 | PF00069 | 0.382 |
MOD_NEK2_1 | 134 | 139 | PF00069 | 0.647 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.621 |
MOD_NEK2_1 | 218 | 223 | PF00069 | 0.635 |
MOD_NEK2_1 | 314 | 319 | PF00069 | 0.637 |
MOD_NEK2_1 | 331 | 336 | PF00069 | 0.597 |
MOD_NEK2_1 | 435 | 440 | PF00069 | 0.350 |
MOD_NEK2_1 | 447 | 452 | PF00069 | 0.349 |
MOD_NEK2_1 | 508 | 513 | PF00069 | 0.595 |
MOD_NEK2_1 | 583 | 588 | PF00069 | 0.585 |
MOD_NEK2_1 | 616 | 621 | PF00069 | 0.578 |
MOD_NEK2_1 | 77 | 82 | PF00069 | 0.350 |
MOD_NEK2_2 | 380 | 385 | PF00069 | 0.553 |
MOD_PIKK_1 | 242 | 248 | PF00454 | 0.613 |
MOD_PKA_2 | 552 | 558 | PF00069 | 0.596 |
MOD_Plk_1 | 280 | 286 | PF00069 | 0.656 |
MOD_Plk_1 | 331 | 337 | PF00069 | 0.619 |
MOD_Plk_1 | 366 | 372 | PF00069 | 0.571 |
MOD_Plk_1 | 443 | 449 | PF00069 | 0.325 |
MOD_Plk_1 | 70 | 76 | PF00069 | 0.343 |
MOD_Plk_4 | 177 | 183 | PF00069 | 0.533 |
MOD_Plk_4 | 214 | 220 | PF00069 | 0.791 |
MOD_Plk_4 | 33 | 39 | PF00069 | 0.234 |
MOD_Plk_4 | 443 | 449 | PF00069 | 0.474 |
MOD_Plk_4 | 461 | 467 | PF00069 | 0.213 |
MOD_ProDKin_1 | 192 | 198 | PF00069 | 0.781 |
MOD_ProDKin_1 | 227 | 233 | PF00069 | 0.733 |
MOD_ProDKin_1 | 289 | 295 | PF00069 | 0.775 |
MOD_ProDKin_1 | 320 | 326 | PF00069 | 0.823 |
MOD_ProDKin_1 | 339 | 345 | PF00069 | 0.614 |
MOD_ProDKin_1 | 358 | 364 | PF00069 | 0.652 |
MOD_ProDKin_1 | 515 | 521 | PF00069 | 0.582 |
MOD_ProDKin_1 | 611 | 617 | PF00069 | 0.635 |
TRG_DiLeu_BaLyEn_6 | 25 | 30 | PF01217 | 0.390 |
TRG_DiLeu_BaLyEn_6 | 45 | 50 | PF01217 | 0.298 |
TRG_ENDOCYTIC_2 | 101 | 104 | PF00928 | 0.532 |
TRG_ENDOCYTIC_2 | 42 | 45 | PF00928 | 0.267 |
TRG_ENDOCYTIC_2 | 427 | 430 | PF00928 | 0.503 |
TRG_ENDOCYTIC_2 | 538 | 541 | PF00928 | 0.535 |
TRG_ENDOCYTIC_2 | 608 | 611 | PF00928 | 0.691 |
TRG_ER_diArg_1 | 515 | 517 | PF00400 | 0.597 |
TRG_ER_diArg_1 | 559 | 561 | PF00400 | 0.710 |
TRG_ER_diArg_1 | 602 | 605 | PF00400 | 0.629 |
TRG_ER_diArg_1 | 620 | 623 | PF00400 | 0.657 |
TRG_NLS_MonoExtN_4 | 588 | 594 | PF00514 | 0.536 |
TRG_Pf-PMV_PEXEL_1 | 546 | 550 | PF00026 | 0.334 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P628 | Leptomonas seymouri | 34% | 97% |
A0A3S7WXW1 | Leishmania donovani | 60% | 99% |
A4I0K3 | Leishmania infantum | 61% | 99% |
E9AWG4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 60% | 99% |
Q4QB07 | Leishmania major | 60% | 100% |