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:0005783 | endoplasmic reticulum | 5 | 2 |
GO:0005794 | Golgi apparatus | 5 | 2 |
GO:0016020 | membrane | 2 | 7 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
Related structures:
AlphaFold database: Q4QB07
Term | Name | Level | Count |
---|---|---|---|
GO:0006497 | protein lipidation | 5 | 2 |
GO:0006605 | protein targeting | 5 | 2 |
GO:0006612 | protein targeting to membrane | 5 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0006810 | transport | 3 | 2 |
GO:0006886 | intracellular protein transport | 4 | 2 |
GO:0008104 | protein localization | 4 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0015031 | protein transport | 4 | 2 |
GO:0018193 | peptidyl-amino acid modification | 5 | 2 |
GO:0018198 | peptidyl-cysteine modification | 6 | 2 |
GO:0018230 | peptidyl-L-cysteine S-palmitoylation | 7 | 2 |
GO:0018231 | peptidyl-S-diacylglycerol-L-cysteine biosynthetic process from peptidyl-cysteine | 7 | 2 |
GO:0018345 | protein palmitoylation | 6 | 2 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0033036 | macromolecule localization | 2 | 2 |
GO:0036211 | protein modification process | 4 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043412 | macromolecule modification | 4 | 2 |
GO:0043543 | protein acylation | 5 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0045184 | establishment of protein localization | 3 | 2 |
GO:0046907 | intracellular transport | 3 | 2 |
GO:0051179 | localization | 1 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
GO:0051641 | cellular localization | 2 | 2 |
GO:0051649 | establishment of localization in cell | 3 | 2 |
GO:0051668 | localization within membrane | 3 | 2 |
GO:0070727 | cellular macromolecule localization | 3 | 2 |
GO:0071702 | organic substance transport | 4 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0071705 | nitrogen compound transport | 4 | 2 |
GO:0072657 | protein localization to membrane | 4 | 2 |
GO:0090150 | establishment of protein localization to membrane | 4 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
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 | 214 | 218 | PF00656 | 0.699 |
CLV_NRD_NRD_1 | 130 | 132 | PF00675 | 0.474 |
CLV_NRD_NRD_1 | 141 | 143 | PF00675 | 0.460 |
CLV_NRD_NRD_1 | 362 | 364 | PF00675 | 0.566 |
CLV_NRD_NRD_1 | 564 | 566 | PF00675 | 0.520 |
CLV_NRD_NRD_1 | 596 | 598 | PF00675 | 0.456 |
CLV_PCSK_KEX2_1 | 130 | 132 | PF00082 | 0.471 |
CLV_PCSK_KEX2_1 | 362 | 364 | PF00082 | 0.566 |
CLV_PCSK_KEX2_1 | 564 | 566 | PF00082 | 0.520 |
CLV_PCSK_KEX2_1 | 596 | 598 | PF00082 | 0.455 |
CLV_PCSK_SKI1_1 | 106 | 110 | PF00082 | 0.388 |
CLV_PCSK_SKI1_1 | 433 | 437 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 600 | 604 | PF00082 | 0.465 |
DEG_APCC_DBOX_1 | 608 | 616 | PF00400 | 0.761 |
DEG_SPOP_SBC_1 | 288 | 292 | PF00917 | 0.798 |
DEG_SPOP_SBC_1 | 304 | 308 | PF00917 | 0.811 |
DEG_SPOP_SBC_1 | 318 | 322 | PF00917 | 0.618 |
DEG_SPOP_SBC_1 | 329 | 333 | PF00917 | 0.711 |
DOC_ANK_TNKS_1 | 578 | 585 | PF00023 | 0.763 |
DOC_CKS1_1 | 1 | 6 | PF01111 | 0.699 |
DOC_MAPK_gen_1 | 130 | 136 | PF00069 | 0.709 |
DOC_MAPK_gen_1 | 596 | 605 | PF00069 | 0.637 |
DOC_MAPK_MEF2A_6 | 26 | 33 | PF00069 | 0.512 |
DOC_MAPK_MEF2A_6 | 372 | 381 | PF00069 | 0.712 |
DOC_PP1_RVXF_1 | 104 | 110 | PF00149 | 0.659 |
DOC_PP1_RVXF_1 | 133 | 139 | PF00149 | 0.705 |
DOC_PP2B_LxvP_1 | 194 | 197 | PF13499 | 0.632 |
DOC_PP2B_LxvP_1 | 553 | 556 | PF13499 | 0.596 |
DOC_PP2B_LxvP_1 | 616 | 619 | PF13499 | 0.692 |
DOC_PP4_FxxP_1 | 109 | 112 | PF00568 | 0.620 |
DOC_PP4_FxxP_1 | 207 | 210 | PF00568 | 0.767 |
DOC_PP4_FxxP_1 | 605 | 608 | PF00568 | 0.655 |
DOC_USP7_MATH_1 | 197 | 201 | PF00917 | 0.762 |
DOC_USP7_MATH_1 | 213 | 217 | PF00917 | 0.712 |
DOC_USP7_MATH_1 | 236 | 240 | PF00917 | 0.811 |
DOC_USP7_MATH_1 | 262 | 266 | PF00917 | 0.642 |
DOC_USP7_MATH_1 | 318 | 322 | PF00917 | 0.796 |
DOC_USP7_MATH_1 | 323 | 327 | PF00917 | 0.709 |
DOC_USP7_MATH_1 | 329 | 333 | PF00917 | 0.741 |
DOC_USP7_MATH_1 | 344 | 348 | PF00917 | 0.737 |
DOC_USP7_MATH_1 | 385 | 389 | PF00917 | 0.634 |
DOC_USP7_MATH_1 | 400 | 404 | PF00917 | 0.546 |
DOC_USP7_MATH_1 | 447 | 451 | PF00917 | 0.450 |
DOC_USP7_MATH_1 | 621 | 625 | PF00917 | 0.786 |
DOC_USP7_MATH_2 | 63 | 69 | PF00917 | 0.503 |
DOC_WW_Pin1_4 | 120 | 125 | PF00397 | 0.709 |
DOC_WW_Pin1_4 | 182 | 187 | PF00397 | 0.711 |
DOC_WW_Pin1_4 | 200 | 205 | PF00397 | 0.689 |
DOC_WW_Pin1_4 | 222 | 227 | PF00397 | 0.820 |
DOC_WW_Pin1_4 | 228 | 233 | PF00397 | 0.762 |
DOC_WW_Pin1_4 | 242 | 247 | PF00397 | 0.621 |
DOC_WW_Pin1_4 | 291 | 296 | PF00397 | 0.824 |
DOC_WW_Pin1_4 | 325 | 330 | PF00397 | 0.828 |
DOC_WW_Pin1_4 | 356 | 361 | PF00397 | 0.661 |
LIG_14-3-3_CanoR_1 | 106 | 112 | PF00244 | 0.585 |
LIG_14-3-3_CanoR_1 | 11 | 16 | PF00244 | 0.724 |
LIG_14-3-3_CanoR_1 | 497 | 503 | PF00244 | 0.546 |
LIG_14-3-3_CanoR_1 | 565 | 574 | PF00244 | 0.740 |
LIG_14-3-3_CanoR_1 | 74 | 78 | PF00244 | 0.457 |
LIG_BIR_III_2 | 352 | 356 | PF00653 | 0.812 |
LIG_BRCT_BRCA1_1 | 387 | 391 | PF00533 | 0.546 |
LIG_BRCT_BRCA1_1 | 449 | 453 | PF00533 | 0.394 |
LIG_BRCT_BRCA1_1 | 509 | 513 | PF00533 | 0.644 |
LIG_CSL_BTD_1 | 471 | 474 | PF09270 | 0.346 |
LIG_deltaCOP1_diTrp_1 | 118 | 126 | PF00928 | 0.672 |
LIG_deltaCOP1_diTrp_1 | 465 | 472 | PF00928 | 0.346 |
LIG_EVH1_1 | 616 | 620 | PF00568 | 0.643 |
LIG_FHA_1 | 1 | 7 | PF00498 | 0.694 |
LIG_FHA_1 | 201 | 207 | PF00498 | 0.656 |
LIG_FHA_1 | 243 | 249 | PF00498 | 0.709 |
LIG_FHA_1 | 34 | 40 | PF00498 | 0.512 |
LIG_FHA_1 | 56 | 62 | PF00498 | 0.529 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.444 |
LIG_FHA_2 | 347 | 353 | PF00498 | 0.833 |
LIG_Integrin_RGD_1 | 579 | 581 | PF01839 | 0.589 |
LIG_LIR_Gen_1 | 450 | 461 | PF02991 | 0.501 |
LIG_LIR_Nem_3 | 14 | 18 | PF02991 | 0.698 |
LIG_LIR_Nem_3 | 388 | 394 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 450 | 456 | PF02991 | 0.502 |
LIG_MYND_1 | 204 | 208 | PF01753 | 0.659 |
LIG_MYND_1 | 356 | 360 | PF01753 | 0.644 |
LIG_NRBOX | 17 | 23 | PF00104 | 0.619 |
LIG_PAM2_1 | 31 | 43 | PF00658 | 0.286 |
LIG_Pex14_2 | 436 | 440 | PF04695 | 0.411 |
LIG_Pex14_2 | 601 | 605 | PF04695 | 0.655 |
LIG_PTAP_UEV_1 | 586 | 591 | PF05743 | 0.786 |
LIG_REV1ctd_RIR_1 | 43 | 52 | PF16727 | 0.424 |
LIG_SH2_CRK | 25 | 29 | PF00017 | 0.475 |
LIG_SH2_CRK | 441 | 445 | PF00017 | 0.394 |
LIG_SH2_CRK | 613 | 617 | PF00017 | 0.771 |
LIG_SH2_SRC | 114 | 117 | PF00017 | 0.597 |
LIG_SH2_STAT5 | 114 | 117 | PF00017 | 0.608 |
LIG_SH2_STAT5 | 122 | 125 | PF00017 | 0.703 |
LIG_SH2_STAT5 | 434 | 437 | PF00017 | 0.512 |
LIG_SH2_STAT5 | 486 | 489 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 79 | 82 | PF00017 | 0.508 |
LIG_SH3_2 | 116 | 121 | PF14604 | 0.702 |
LIG_SH3_2 | 275 | 280 | PF14604 | 0.647 |
LIG_SH3_3 | 113 | 119 | PF00018 | 0.689 |
LIG_SH3_3 | 223 | 229 | PF00018 | 0.754 |
LIG_SH3_3 | 272 | 278 | PF00018 | 0.676 |
LIG_SH3_3 | 514 | 520 | PF00018 | 0.702 |
LIG_SH3_3 | 522 | 528 | PF00018 | 0.726 |
LIG_SH3_3 | 584 | 590 | PF00018 | 0.832 |
LIG_SH3_3 | 614 | 620 | PF00018 | 0.711 |
LIG_TRAF2_1 | 159 | 162 | PF00917 | 0.659 |
LIG_TRFH_1 | 613 | 617 | PF08558 | 0.771 |
LIG_TYR_ITIM | 439 | 444 | PF00017 | 0.394 |
LIG_TYR_ITIM | 484 | 489 | PF00017 | 0.450 |
LIG_TYR_ITIM | 99 | 104 | PF00017 | 0.336 |
MOD_CDC14_SPxK_1 | 359 | 362 | PF00782 | 0.645 |
MOD_CDK_SPK_2 | 120 | 125 | PF00069 | 0.725 |
MOD_CDK_SPxK_1 | 356 | 362 | PF00069 | 0.645 |
MOD_CDK_SPxxK_3 | 356 | 363 | PF00069 | 0.645 |
MOD_CK1_1 | 185 | 191 | PF00069 | 0.674 |
MOD_CK1_1 | 200 | 206 | PF00069 | 0.669 |
MOD_CK1_1 | 291 | 297 | PF00069 | 0.747 |
MOD_CK1_1 | 314 | 320 | PF00069 | 0.764 |
MOD_CK1_1 | 321 | 327 | PF00069 | 0.799 |
MOD_CK1_1 | 332 | 338 | PF00069 | 0.772 |
MOD_CK1_1 | 347 | 353 | PF00069 | 0.626 |
MOD_CK1_1 | 530 | 536 | PF00069 | 0.676 |
MOD_CK1_1 | 572 | 578 | PF00069 | 0.800 |
MOD_CK1_1 | 588 | 594 | PF00069 | 0.783 |
MOD_CK2_1 | 293 | 299 | PF00069 | 0.764 |
MOD_CK2_1 | 497 | 503 | PF00069 | 0.534 |
MOD_CK2_1 | 513 | 519 | PF00069 | 0.670 |
MOD_GlcNHglycan | 138 | 141 | PF01048 | 0.505 |
MOD_GlcNHglycan | 187 | 190 | PF01048 | 0.547 |
MOD_GlcNHglycan | 199 | 202 | PF01048 | 0.514 |
MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.519 |
MOD_GlcNHglycan | 272 | 275 | PF01048 | 0.590 |
MOD_GlcNHglycan | 284 | 287 | PF01048 | 0.515 |
MOD_GlcNHglycan | 295 | 298 | PF01048 | 0.412 |
MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.603 |
MOD_GlcNHglycan | 321 | 324 | PF01048 | 0.579 |
MOD_GlcNHglycan | 325 | 328 | PF01048 | 0.555 |
MOD_GlcNHglycan | 33 | 36 | PF01048 | 0.411 |
MOD_GlcNHglycan | 576 | 579 | PF01048 | 0.571 |
MOD_GlcNHglycan | 587 | 590 | PF01048 | 0.539 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.792 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.704 |
MOD_GSK3_1 | 236 | 243 | PF00069 | 0.763 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.712 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.653 |
MOD_GSK3_1 | 303 | 310 | PF00069 | 0.733 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.724 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.685 |
MOD_GSK3_1 | 503 | 510 | PF00069 | 0.659 |
MOD_GSK3_1 | 569 | 576 | PF00069 | 0.804 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.488 |
MOD_LATS_1 | 361 | 367 | PF00433 | 0.768 |
MOD_N-GLC_2 | 424 | 426 | PF02516 | 0.338 |
MOD_NEK2_1 | 100 | 105 | PF00069 | 0.466 |
MOD_NEK2_1 | 134 | 139 | PF00069 | 0.749 |
MOD_NEK2_1 | 33 | 38 | PF00069 | 0.286 |
MOD_NEK2_1 | 440 | 445 | PF00069 | 0.377 |
MOD_NEK2_1 | 452 | 457 | PF00069 | 0.411 |
MOD_NEK2_1 | 513 | 518 | PF00069 | 0.671 |
MOD_NEK2_1 | 566 | 571 | PF00069 | 0.736 |
MOD_NEK2_1 | 573 | 578 | PF00069 | 0.781 |
MOD_NEK2_1 | 77 | 82 | PF00069 | 0.458 |
MOD_NEK2_2 | 385 | 390 | PF00069 | 0.626 |
MOD_PIKK_1 | 520 | 526 | PF00454 | 0.727 |
MOD_PIKK_1 | 622 | 628 | PF00454 | 0.682 |
MOD_PKA_2 | 335 | 341 | PF00069 | 0.799 |
MOD_PKA_2 | 503 | 509 | PF00069 | 0.574 |
MOD_PKA_2 | 73 | 79 | PF00069 | 0.452 |
MOD_Plk_1 | 250 | 256 | PF00069 | 0.789 |
MOD_Plk_4 | 215 | 221 | PF00069 | 0.838 |
MOD_Plk_4 | 447 | 453 | PF00069 | 0.501 |
MOD_Plk_4 | 457 | 463 | PF00069 | 0.308 |
MOD_Plk_4 | 569 | 575 | PF00069 | 0.672 |
MOD_Plk_4 | 65 | 71 | PF00069 | 0.466 |
MOD_ProDKin_1 | 120 | 126 | PF00069 | 0.707 |
MOD_ProDKin_1 | 182 | 188 | PF00069 | 0.712 |
MOD_ProDKin_1 | 200 | 206 | PF00069 | 0.692 |
MOD_ProDKin_1 | 222 | 228 | PF00069 | 0.819 |
MOD_ProDKin_1 | 242 | 248 | PF00069 | 0.677 |
MOD_ProDKin_1 | 291 | 297 | PF00069 | 0.824 |
MOD_ProDKin_1 | 325 | 331 | PF00069 | 0.830 |
MOD_ProDKin_1 | 356 | 362 | PF00069 | 0.662 |
TRG_DiLeu_BaEn_1 | 65 | 70 | PF01217 | 0.466 |
TRG_DiLeu_BaLyEn_6 | 25 | 30 | PF01217 | 0.512 |
TRG_DiLeu_BaLyEn_6 | 45 | 50 | PF01217 | 0.253 |
TRG_ENDOCYTIC_2 | 101 | 104 | PF00928 | 0.561 |
TRG_ENDOCYTIC_2 | 42 | 45 | PF00928 | 0.378 |
TRG_ENDOCYTIC_2 | 432 | 435 | PF00928 | 0.546 |
TRG_ENDOCYTIC_2 | 441 | 444 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 486 | 489 | PF00928 | 0.450 |
TRG_ENDOCYTIC_2 | 613 | 616 | PF00928 | 0.765 |
TRG_ER_diArg_1 | 10 | 13 | PF00400 | 0.669 |
TRG_ER_diArg_1 | 362 | 364 | PF00400 | 0.766 |
TRG_ER_diArg_1 | 564 | 566 | PF00400 | 0.791 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P628 | Leptomonas seymouri | 36% | 98% |
A0A3S7WXW1 | Leishmania donovani | 90% | 100% |
A4HD17 | Leishmania braziliensis | 60% | 100% |
A4I0K3 | Leishmania infantum | 91% | 100% |
E9AWG4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |