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: A4I0K3
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_NRD_NRD_1 | 130 | 132 | PF00675 | 0.408 |
CLV_NRD_NRD_1 | 154 | 156 | PF00675 | 0.355 |
CLV_NRD_NRD_1 | 361 | 363 | PF00675 | 0.494 |
CLV_NRD_NRD_1 | 563 | 565 | PF00675 | 0.534 |
CLV_NRD_NRD_1 | 595 | 597 | PF00675 | 0.526 |
CLV_PCSK_KEX2_1 | 130 | 132 | PF00082 | 0.408 |
CLV_PCSK_KEX2_1 | 153 | 155 | PF00082 | 0.342 |
CLV_PCSK_KEX2_1 | 361 | 363 | PF00082 | 0.494 |
CLV_PCSK_KEX2_1 | 563 | 565 | PF00082 | 0.534 |
CLV_PCSK_KEX2_1 | 595 | 597 | PF00082 | 0.503 |
CLV_PCSK_SKI1_1 | 106 | 110 | PF00082 | 0.370 |
CLV_PCSK_SKI1_1 | 154 | 158 | PF00082 | 0.335 |
CLV_PCSK_SKI1_1 | 410 | 414 | PF00082 | 0.294 |
CLV_PCSK_SKI1_1 | 432 | 436 | PF00082 | 0.337 |
CLV_PCSK_SKI1_1 | 599 | 603 | PF00082 | 0.403 |
DEG_APCC_DBOX_1 | 153 | 161 | PF00400 | 0.531 |
DEG_APCC_DBOX_1 | 607 | 615 | PF00400 | 0.627 |
DEG_SPOP_SBC_1 | 287 | 291 | PF00917 | 0.756 |
DEG_SPOP_SBC_1 | 303 | 307 | PF00917 | 0.660 |
DEG_SPOP_SBC_1 | 328 | 332 | PF00917 | 0.705 |
DOC_ANK_TNKS_1 | 577 | 584 | PF00023 | 0.736 |
DOC_CDC14_PxL_1 | 241 | 249 | PF14671 | 0.647 |
DOC_CKS1_1 | 1 | 6 | PF01111 | 0.612 |
DOC_CYCLIN_yCln2_LP_2 | 193 | 199 | PF00134 | 0.636 |
DOC_MAPK_gen_1 | 130 | 136 | PF00069 | 0.608 |
DOC_MAPK_gen_1 | 595 | 604 | PF00069 | 0.633 |
DOC_MAPK_MEF2A_6 | 26 | 33 | PF00069 | 0.392 |
DOC_MAPK_MEF2A_6 | 371 | 380 | PF00069 | 0.607 |
DOC_MAPK_RevD_3 | 140 | 154 | PF00069 | 0.529 |
DOC_PP1_RVXF_1 | 104 | 110 | PF00149 | 0.569 |
DOC_PP1_RVXF_1 | 133 | 139 | PF00149 | 0.604 |
DOC_PP2B_LxvP_1 | 617 | 620 | PF13499 | 0.609 |
DOC_PP4_FxxP_1 | 109 | 112 | PF00568 | 0.646 |
DOC_PP4_FxxP_1 | 206 | 209 | PF00568 | 0.722 |
DOC_PP4_FxxP_1 | 604 | 607 | PF00568 | 0.611 |
DOC_USP7_MATH_1 | 212 | 216 | PF00917 | 0.690 |
DOC_USP7_MATH_1 | 235 | 239 | PF00917 | 0.751 |
DOC_USP7_MATH_1 | 311 | 315 | PF00917 | 0.712 |
DOC_USP7_MATH_1 | 322 | 326 | PF00917 | 0.696 |
DOC_USP7_MATH_1 | 328 | 332 | PF00917 | 0.665 |
DOC_USP7_MATH_1 | 384 | 388 | PF00917 | 0.591 |
DOC_USP7_MATH_1 | 399 | 403 | PF00917 | 0.434 |
DOC_USP7_MATH_1 | 446 | 450 | PF00917 | 0.356 |
DOC_USP7_MATH_1 | 573 | 577 | PF00917 | 0.680 |
DOC_USP7_MATH_1 | 620 | 624 | PF00917 | 0.692 |
DOC_USP7_MATH_2 | 63 | 69 | PF00917 | 0.418 |
DOC_WW_Pin1_4 | 120 | 125 | PF00397 | 0.625 |
DOC_WW_Pin1_4 | 192 | 197 | PF00397 | 0.792 |
DOC_WW_Pin1_4 | 199 | 204 | PF00397 | 0.725 |
DOC_WW_Pin1_4 | 221 | 226 | PF00397 | 0.784 |
DOC_WW_Pin1_4 | 227 | 232 | PF00397 | 0.779 |
DOC_WW_Pin1_4 | 290 | 295 | PF00397 | 0.771 |
DOC_WW_Pin1_4 | 324 | 329 | PF00397 | 0.809 |
DOC_WW_Pin1_4 | 569 | 574 | PF00397 | 0.670 |
DOC_WW_Pin1_4 | 615 | 620 | PF00397 | 0.630 |
LIG_14-3-3_CanoR_1 | 106 | 112 | PF00244 | 0.569 |
LIG_14-3-3_CanoR_1 | 11 | 16 | PF00244 | 0.638 |
LIG_14-3-3_CanoR_1 | 239 | 247 | PF00244 | 0.648 |
LIG_14-3-3_CanoR_1 | 361 | 370 | PF00244 | 0.642 |
LIG_14-3-3_CanoR_1 | 496 | 502 | PF00244 | 0.578 |
LIG_14-3-3_CanoR_1 | 564 | 573 | PF00244 | 0.723 |
LIG_14-3-3_CanoR_1 | 74 | 78 | PF00244 | 0.360 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.594 |
LIG_BIR_III_2 | 351 | 355 | PF00653 | 0.740 |
LIG_BRCT_BRCA1_1 | 386 | 390 | PF00533 | 0.537 |
LIG_BRCT_BRCA1_1 | 448 | 452 | PF00533 | 0.356 |
LIG_BRCT_BRCA1_1 | 508 | 512 | PF00533 | 0.608 |
LIG_CSL_BTD_1 | 470 | 473 | PF09270 | 0.337 |
LIG_deltaCOP1_diTrp_1 | 117 | 126 | PF00928 | 0.586 |
LIG_deltaCOP1_diTrp_1 | 464 | 471 | PF00928 | 0.337 |
LIG_FHA_1 | 1 | 7 | PF00498 | 0.608 |
LIG_FHA_1 | 34 | 40 | PF00498 | 0.439 |
LIG_FHA_1 | 448 | 454 | PF00498 | 0.347 |
LIG_FHA_1 | 57 | 63 | PF00498 | 0.427 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.407 |
LIG_FHA_2 | 346 | 352 | PF00498 | 0.748 |
LIG_Integrin_RGD_1 | 578 | 580 | PF01839 | 0.556 |
LIG_LIR_Gen_1 | 103 | 112 | PF02991 | 0.618 |
LIG_LIR_Gen_1 | 449 | 460 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 103 | 107 | PF02991 | 0.612 |
LIG_LIR_Nem_3 | 14 | 18 | PF02991 | 0.617 |
LIG_LIR_Nem_3 | 387 | 393 | PF02991 | 0.537 |
LIG_LIR_Nem_3 | 449 | 455 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 466 | 472 | PF02991 | 0.234 |
LIG_NRBOX | 17 | 23 | PF00104 | 0.569 |
LIG_Pex14_2 | 435 | 439 | PF04695 | 0.392 |
LIG_Pex14_2 | 600 | 604 | PF04695 | 0.574 |
LIG_PTAP_UEV_1 | 585 | 590 | PF05743 | 0.733 |
LIG_REV1ctd_RIR_1 | 43 | 52 | PF16727 | 0.368 |
LIG_SH2_CRK | 25 | 29 | PF00017 | 0.442 |
LIG_SH2_CRK | 440 | 444 | PF00017 | 0.489 |
LIG_SH2_CRK | 612 | 616 | PF00017 | 0.691 |
LIG_SH2_STAT5 | 114 | 117 | PF00017 | 0.568 |
LIG_SH2_STAT5 | 122 | 125 | PF00017 | 0.564 |
LIG_SH2_STAT5 | 433 | 436 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 485 | 488 | PF00017 | 0.378 |
LIG_SH2_STAT5 | 75 | 78 | PF00017 | 0.400 |
LIG_SH2_STAT5 | 79 | 82 | PF00017 | 0.371 |
LIG_SH3_2 | 116 | 121 | PF14604 | 0.587 |
LIG_SH3_3 | 113 | 119 | PF00018 | 0.679 |
LIG_SH3_3 | 193 | 199 | PF00018 | 0.664 |
LIG_SH3_3 | 222 | 228 | PF00018 | 0.788 |
LIG_SH3_3 | 340 | 346 | PF00018 | 0.701 |
LIG_SH3_3 | 521 | 527 | PF00018 | 0.672 |
LIG_SH3_3 | 583 | 589 | PF00018 | 0.764 |
LIG_SH3_3 | 613 | 619 | PF00018 | 0.616 |
LIG_SH3_CIN85_PxpxPR_1 | 626 | 631 | PF14604 | 0.690 |
LIG_TRAF2_1 | 159 | 162 | PF00917 | 0.582 |
LIG_TRFH_1 | 612 | 616 | PF08558 | 0.606 |
LIG_TYR_ITIM | 438 | 443 | PF00017 | 0.489 |
LIG_TYR_ITIM | 483 | 488 | PF00017 | 0.356 |
LIG_WRC_WIRS_1 | 101 | 106 | PF05994 | 0.376 |
MOD_CDK_SPK_2 | 120 | 125 | PF00069 | 0.587 |
MOD_CDK_SPxK_1 | 329 | 335 | PF00069 | 0.760 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.572 |
MOD_CK1_1 | 214 | 220 | PF00069 | 0.694 |
MOD_CK1_1 | 290 | 296 | PF00069 | 0.759 |
MOD_CK1_1 | 313 | 319 | PF00069 | 0.751 |
MOD_CK1_1 | 320 | 326 | PF00069 | 0.713 |
MOD_CK1_1 | 519 | 525 | PF00069 | 0.671 |
MOD_CK1_1 | 529 | 535 | PF00069 | 0.661 |
MOD_CK1_1 | 571 | 577 | PF00069 | 0.747 |
MOD_CK1_1 | 587 | 593 | PF00069 | 0.612 |
MOD_CK2_1 | 292 | 298 | PF00069 | 0.827 |
MOD_CK2_1 | 496 | 502 | PF00069 | 0.606 |
MOD_CK2_1 | 512 | 518 | PF00069 | 0.549 |
MOD_Cter_Amidation | 593 | 596 | PF01082 | 0.373 |
MOD_GlcNHglycan | 138 | 141 | PF01048 | 0.401 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.506 |
MOD_GlcNHglycan | 271 | 274 | PF01048 | 0.510 |
MOD_GlcNHglycan | 282 | 286 | PF01048 | 0.506 |
MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.536 |
MOD_GlcNHglycan | 320 | 323 | PF01048 | 0.545 |
MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.530 |
MOD_GlcNHglycan | 33 | 36 | PF01048 | 0.392 |
MOD_GlcNHglycan | 479 | 482 | PF01048 | 0.296 |
MOD_GlcNHglycan | 518 | 521 | PF01048 | 0.475 |
MOD_GlcNHglycan | 575 | 578 | PF01048 | 0.572 |
MOD_GlcNHglycan | 586 | 589 | PF01048 | 0.486 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.737 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.752 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.774 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.776 |
MOD_GSK3_1 | 299 | 306 | PF00069 | 0.723 |
MOD_GSK3_1 | 307 | 314 | PF00069 | 0.707 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.688 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.665 |
MOD_GSK3_1 | 447 | 454 | PF00069 | 0.412 |
MOD_GSK3_1 | 502 | 509 | PF00069 | 0.651 |
MOD_GSK3_1 | 512 | 519 | PF00069 | 0.592 |
MOD_GSK3_1 | 565 | 572 | PF00069 | 0.742 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.408 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.385 |
MOD_LATS_1 | 360 | 366 | PF00433 | 0.691 |
MOD_N-GLC_1 | 447 | 452 | PF02516 | 0.332 |
MOD_N-GLC_2 | 423 | 425 | PF02516 | 0.415 |
MOD_NEK2_1 | 100 | 105 | PF00069 | 0.497 |
MOD_NEK2_1 | 134 | 139 | PF00069 | 0.628 |
MOD_NEK2_1 | 439 | 444 | PF00069 | 0.522 |
MOD_NEK2_1 | 451 | 456 | PF00069 | 0.326 |
MOD_NEK2_1 | 512 | 517 | PF00069 | 0.637 |
MOD_NEK2_1 | 552 | 557 | PF00069 | 0.604 |
MOD_NEK2_1 | 565 | 570 | PF00069 | 0.687 |
MOD_NEK2_1 | 69 | 74 | PF00069 | 0.400 |
MOD_NEK2_1 | 77 | 82 | PF00069 | 0.395 |
MOD_NEK2_2 | 355 | 360 | PF00069 | 0.651 |
MOD_NEK2_2 | 384 | 389 | PF00069 | 0.602 |
MOD_PIKK_1 | 519 | 525 | PF00454 | 0.671 |
MOD_PIKK_1 | 69 | 75 | PF00454 | 0.344 |
MOD_PKA_2 | 334 | 340 | PF00069 | 0.751 |
MOD_PKA_2 | 502 | 508 | PF00069 | 0.512 |
MOD_PKA_2 | 73 | 79 | PF00069 | 0.358 |
MOD_Plk_1 | 249 | 255 | PF00069 | 0.693 |
MOD_Plk_1 | 447 | 453 | PF00069 | 0.332 |
MOD_Plk_4 | 214 | 220 | PF00069 | 0.797 |
MOD_Plk_4 | 447 | 453 | PF00069 | 0.489 |
MOD_Plk_4 | 456 | 462 | PF00069 | 0.337 |
MOD_Plk_4 | 65 | 71 | PF00069 | 0.398 |
MOD_ProDKin_1 | 120 | 126 | PF00069 | 0.629 |
MOD_ProDKin_1 | 192 | 198 | PF00069 | 0.792 |
MOD_ProDKin_1 | 199 | 205 | PF00069 | 0.728 |
MOD_ProDKin_1 | 221 | 227 | PF00069 | 0.784 |
MOD_ProDKin_1 | 290 | 296 | PF00069 | 0.770 |
MOD_ProDKin_1 | 324 | 330 | PF00069 | 0.810 |
MOD_ProDKin_1 | 569 | 575 | PF00069 | 0.672 |
MOD_ProDKin_1 | 615 | 621 | PF00069 | 0.641 |
TRG_DiLeu_BaEn_1 | 65 | 70 | PF01217 | 0.402 |
TRG_DiLeu_BaLyEn_6 | 25 | 30 | PF01217 | 0.392 |
TRG_DiLeu_BaLyEn_6 | 45 | 50 | PF01217 | 0.302 |
TRG_ENDOCYTIC_2 | 101 | 104 | PF00928 | 0.541 |
TRG_ENDOCYTIC_2 | 431 | 434 | PF00928 | 0.632 |
TRG_ENDOCYTIC_2 | 440 | 443 | PF00928 | 0.379 |
TRG_ENDOCYTIC_2 | 485 | 488 | PF00928 | 0.356 |
TRG_ENDOCYTIC_2 | 612 | 615 | PF00928 | 0.697 |
TRG_ER_diArg_1 | 10 | 13 | PF00400 | 0.627 |
TRG_ER_diArg_1 | 152 | 155 | PF00400 | 0.541 |
TRG_ER_diArg_1 | 361 | 363 | PF00400 | 0.694 |
TRG_ER_diArg_1 | 563 | 565 | PF00400 | 0.733 |
TRG_ER_diArg_1 | 626 | 629 | PF00400 | 0.717 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WXW1 | Leishmania donovani | 99% | 100% |
A4HD17 | Leishmania braziliensis | 61% | 99% |
E9AWG3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9AWG4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
Q4QB07 | Leishmania major | 91% | 100% |