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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005789 | endoplasmic reticulum membrane | 4 | 7 |
GO:0016020 | membrane | 2 | 7 |
GO:0031090 | organelle membrane | 3 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0031501 | mannosyltransferase complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0140535 | intracellular protein-containing complex | 2 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1990234 | transferase complex | 3 | 1 |
Related structures:
AlphaFold database: A4H9K3
Term | Name | Level | Count |
---|---|---|---|
GO:0006497 | protein lipidation | 5 | 7 |
GO:0006505 | GPI anchor metabolic process | 6 | 7 |
GO:0006506 | GPI anchor biosynthetic process | 6 | 7 |
GO:0006629 | lipid metabolic process | 3 | 7 |
GO:0006643 | membrane lipid metabolic process | 4 | 7 |
GO:0006644 | phospholipid metabolic process | 4 | 7 |
GO:0006650 | glycerophospholipid metabolic process | 5 | 7 |
GO:0006661 | phosphatidylinositol biosynthetic process | 6 | 7 |
GO:0006664 | glycolipid metabolic process | 5 | 7 |
GO:0006793 | phosphorus metabolic process | 3 | 7 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 7 |
GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0008610 | lipid biosynthetic process | 4 | 7 |
GO:0008654 | phospholipid biosynthetic process | 5 | 7 |
GO:0009058 | biosynthetic process | 2 | 7 |
GO:0009247 | glycolipid biosynthetic process | 5 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0019538 | protein metabolic process | 3 | 7 |
GO:0019637 | organophosphate metabolic process | 3 | 7 |
GO:0036211 | protein modification process | 4 | 7 |
GO:0043170 | macromolecule metabolic process | 3 | 7 |
GO:0043412 | macromolecule modification | 4 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0044249 | cellular biosynthetic process | 3 | 7 |
GO:0044255 | cellular lipid metabolic process | 3 | 7 |
GO:0045017 | glycerolipid biosynthetic process | 4 | 7 |
GO:0046467 | membrane lipid biosynthetic process | 4 | 7 |
GO:0046474 | glycerophospholipid biosynthetic process | 5 | 7 |
GO:0046486 | glycerolipid metabolic process | 4 | 7 |
GO:0046488 | phosphatidylinositol metabolic process | 6 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:0090407 | organophosphate biosynthetic process | 4 | 7 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 7 |
GO:1901137 | carbohydrate derivative biosynthetic process | 4 | 7 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 7 |
GO:1901576 | organic substance biosynthetic process | 3 | 7 |
GO:1903509 | liposaccharide metabolic process | 4 | 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000009 | alpha-1,6-mannosyltransferase activity | 6 | 7 |
GO:0000030 | mannosyltransferase activity | 5 | 7 |
GO:0003824 | catalytic activity | 1 | 7 |
GO:0004376 | glycolipid mannosyltransferase activity | 6 | 7 |
GO:0016740 | transferase activity | 2 | 7 |
GO:0016757 | glycosyltransferase activity | 3 | 7 |
GO:0016758 | hexosyltransferase activity | 4 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 233 | 237 | PF00656 | 0.571 |
CLV_NRD_NRD_1 | 164 | 166 | PF00675 | 0.276 |
CLV_NRD_NRD_1 | 259 | 261 | PF00675 | 0.276 |
CLV_PCSK_FUR_1 | 257 | 261 | PF00082 | 0.304 |
CLV_PCSK_KEX2_1 | 164 | 166 | PF00082 | 0.276 |
CLV_PCSK_KEX2_1 | 187 | 189 | PF00082 | 0.433 |
CLV_PCSK_KEX2_1 | 257 | 259 | PF00082 | 0.340 |
CLV_PCSK_PC1ET2_1 | 187 | 189 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 164 | 168 | PF00082 | 0.333 |
CLV_PCSK_SKI1_1 | 184 | 188 | PF00082 | 0.434 |
CLV_PCSK_SKI1_1 | 373 | 377 | PF00082 | 0.461 |
CLV_PCSK_SKI1_1 | 50 | 54 | PF00082 | 0.393 |
CLV_PCSK_SKI1_1 | 511 | 515 | PF00082 | 0.476 |
CLV_PCSK_SKI1_1 | 584 | 588 | PF00082 | 0.266 |
DEG_APCC_DBOX_1 | 474 | 482 | PF00400 | 0.633 |
DEG_APCC_DBOX_1 | 49 | 57 | PF00400 | 0.314 |
DEG_ODPH_VHL_1 | 134 | 146 | PF01847 | 0.238 |
DEG_SCF_FBW7_2 | 189 | 196 | PF00400 | 0.723 |
DEG_SPOP_SBC_1 | 325 | 329 | PF00917 | 0.624 |
DOC_CDC14_PxL_1 | 117 | 125 | PF14671 | 0.314 |
DOC_CDC14_PxL_1 | 365 | 373 | PF14671 | 0.601 |
DOC_CKS1_1 | 270 | 275 | PF01111 | 0.314 |
DOC_CKS1_1 | 319 | 324 | PF01111 | 0.605 |
DOC_CYCLIN_yCln2_LP_2 | 420 | 426 | PF00134 | 0.393 |
DOC_CYCLIN_yCln2_LP_2 | 428 | 434 | PF00134 | 0.308 |
DOC_CYCLIN_yCln2_LP_2 | 559 | 565 | PF00134 | 0.314 |
DOC_MAPK_gen_1 | 164 | 171 | PF00069 | 0.476 |
DOC_MAPK_gen_1 | 538 | 545 | PF00069 | 0.316 |
DOC_MAPK_MEF2A_6 | 480 | 489 | PF00069 | 0.488 |
DOC_PP2B_LxvP_1 | 235 | 238 | PF13499 | 0.611 |
DOC_PP2B_LxvP_1 | 338 | 341 | PF13499 | 0.734 |
DOC_PP2B_LxvP_1 | 428 | 431 | PF13499 | 0.233 |
DOC_PP2B_LxvP_1 | 474 | 477 | PF13499 | 0.657 |
DOC_PP2B_LxvP_1 | 559 | 562 | PF13499 | 0.314 |
DOC_PP4_FxxP_1 | 171 | 174 | PF00568 | 0.476 |
DOC_PP4_FxxP_1 | 68 | 71 | PF00568 | 0.537 |
DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.288 |
DOC_USP7_MATH_1 | 377 | 381 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 436 | 440 | PF00917 | 0.609 |
DOC_USP7_MATH_1 | 443 | 447 | PF00917 | 0.582 |
DOC_USP7_MATH_1 | 548 | 552 | PF00917 | 0.224 |
DOC_USP7_MATH_1 | 71 | 75 | PF00917 | 0.504 |
DOC_WW_Pin1_4 | 189 | 194 | PF00397 | 0.761 |
DOC_WW_Pin1_4 | 269 | 274 | PF00397 | 0.314 |
DOC_WW_Pin1_4 | 318 | 323 | PF00397 | 0.667 |
DOC_WW_Pin1_4 | 373 | 378 | PF00397 | 0.685 |
DOC_WW_Pin1_4 | 585 | 590 | PF00397 | 0.440 |
LIG_14-3-3_CanoR_1 | 14 | 20 | PF00244 | 0.272 |
LIG_14-3-3_CanoR_1 | 182 | 189 | PF00244 | 0.673 |
LIG_14-3-3_CanoR_1 | 311 | 316 | PF00244 | 0.664 |
LIG_14-3-3_CanoR_1 | 584 | 589 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 595 | 603 | PF00244 | 0.403 |
LIG_14-3-3_CanoR_1 | 654 | 659 | PF00244 | 0.418 |
LIG_14-3-3_CanoR_1 | 88 | 92 | PF00244 | 0.533 |
LIG_Actin_WH2_2 | 569 | 586 | PF00022 | 0.241 |
LIG_APCC_ABBA_1 | 279 | 284 | PF00400 | 0.329 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.581 |
LIG_BRCT_BRCA1_1 | 410 | 414 | PF00533 | 0.276 |
LIG_BRCT_BRCA1_1 | 550 | 554 | PF00533 | 0.224 |
LIG_BRCT_BRCA1_1 | 73 | 77 | PF00533 | 0.503 |
LIG_CaM_NSCaTE_8 | 541 | 548 | PF13499 | 0.333 |
LIG_DLG_GKlike_1 | 311 | 319 | PF00625 | 0.621 |
LIG_FHA_1 | 129 | 135 | PF00498 | 0.279 |
LIG_FHA_1 | 229 | 235 | PF00498 | 0.645 |
LIG_FHA_1 | 276 | 282 | PF00498 | 0.301 |
LIG_FHA_1 | 350 | 356 | PF00498 | 0.669 |
LIG_FHA_1 | 38 | 44 | PF00498 | 0.333 |
LIG_FHA_1 | 654 | 660 | PF00498 | 0.421 |
LIG_FHA_2 | 231 | 237 | PF00498 | 0.553 |
LIG_FHA_2 | 245 | 251 | PF00498 | 0.581 |
LIG_FHA_2 | 318 | 324 | PF00498 | 0.601 |
LIG_FHA_2 | 34 | 40 | PF00498 | 0.375 |
LIG_FHA_2 | 77 | 83 | PF00498 | 0.559 |
LIG_GBD_Chelix_1 | 158 | 166 | PF00786 | 0.233 |
LIG_GBD_Chelix_1 | 397 | 405 | PF00786 | 0.393 |
LIG_GBD_Chelix_1 | 48 | 56 | PF00786 | 0.393 |
LIG_GBD_Chelix_1 | 617 | 625 | PF00786 | 0.241 |
LIG_LIR_Apic_2 | 170 | 174 | PF02991 | 0.476 |
LIG_LIR_Gen_1 | 198 | 209 | PF02991 | 0.601 |
LIG_LIR_Gen_1 | 27 | 34 | PF02991 | 0.343 |
LIG_LIR_Gen_1 | 284 | 295 | PF02991 | 0.241 |
LIG_LIR_Gen_1 | 86 | 96 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 27 | 31 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 284 | 290 | PF02991 | 0.241 |
LIG_LIR_Nem_3 | 291 | 296 | PF02991 | 0.221 |
LIG_LIR_Nem_3 | 415 | 419 | PF02991 | 0.299 |
LIG_LIR_Nem_3 | 544 | 549 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 551 | 557 | PF02991 | 0.315 |
LIG_LIR_Nem_3 | 86 | 92 | PF02991 | 0.476 |
LIG_LYPXL_S_1 | 532 | 536 | PF13949 | 0.476 |
LIG_LYPXL_yS_3 | 533 | 536 | PF13949 | 0.276 |
LIG_MYND_1 | 472 | 476 | PF01753 | 0.663 |
LIG_NRBOX | 616 | 622 | PF00104 | 0.289 |
LIG_NRBOX | 642 | 648 | PF00104 | 0.314 |
LIG_PCNA_PIPBox_1 | 309 | 318 | PF02747 | 0.670 |
LIG_Pex14_1 | 387 | 391 | PF04695 | 0.598 |
LIG_RPA_C_Fungi | 254 | 266 | PF08784 | 0.393 |
LIG_RPA_C_Fungi | 9 | 21 | PF08784 | 0.241 |
LIG_SH2_NCK_1 | 549 | 553 | PF00017 | 0.241 |
LIG_SH2_PTP2 | 147 | 150 | PF00017 | 0.393 |
LIG_SH2_SRC | 84 | 87 | PF00017 | 0.501 |
LIG_SH2_STAP1 | 282 | 286 | PF00017 | 0.314 |
LIG_SH2_STAP1 | 434 | 438 | PF00017 | 0.343 |
LIG_SH2_STAT3 | 434 | 437 | PF00017 | 0.382 |
LIG_SH2_STAT5 | 108 | 111 | PF00017 | 0.314 |
LIG_SH2_STAT5 | 147 | 150 | PF00017 | 0.478 |
LIG_SH2_STAT5 | 282 | 285 | PF00017 | 0.330 |
LIG_SH2_STAT5 | 296 | 299 | PF00017 | 0.314 |
LIG_SH2_STAT5 | 315 | 318 | PF00017 | 0.515 |
LIG_SH2_STAT5 | 33 | 36 | PF00017 | 0.356 |
LIG_SH2_STAT5 | 501 | 504 | PF00017 | 0.314 |
LIG_SH2_STAT5 | 506 | 509 | PF00017 | 0.314 |
LIG_SH2_STAT5 | 549 | 552 | PF00017 | 0.314 |
LIG_SH2_STAT5 | 575 | 578 | PF00017 | 0.304 |
LIG_SH2_STAT6 | 508 | 512 | PF00017 | 0.264 |
LIG_SH3_1 | 337 | 343 | PF00018 | 0.666 |
LIG_SH3_3 | 112 | 118 | PF00018 | 0.317 |
LIG_SH3_3 | 16 | 22 | PF00018 | 0.428 |
LIG_SH3_3 | 267 | 273 | PF00018 | 0.241 |
LIG_SH3_3 | 337 | 343 | PF00018 | 0.666 |
LIG_SH3_3 | 363 | 369 | PF00018 | 0.492 |
LIG_SH3_3 | 494 | 500 | PF00018 | 0.403 |
LIG_SUMO_SIM_anti_2 | 660 | 666 | PF11976 | 0.304 |
LIG_SUMO_SIM_par_1 | 120 | 126 | PF11976 | 0.241 |
LIG_SUMO_SIM_par_1 | 244 | 250 | PF11976 | 0.385 |
LIG_SUMO_SIM_par_1 | 277 | 285 | PF11976 | 0.249 |
LIG_SUMO_SIM_par_1 | 488 | 493 | PF11976 | 0.314 |
LIG_SUMO_SIM_par_1 | 561 | 567 | PF11976 | 0.393 |
LIG_SxIP_EBH_1 | 362 | 371 | PF03271 | 0.647 |
LIG_TRAF2_1 | 79 | 82 | PF00917 | 0.422 |
LIG_TRFH_1 | 574 | 578 | PF08558 | 0.241 |
LIG_WRC_WIRS_1 | 168 | 173 | PF05994 | 0.314 |
MOD_CK1_1 | 195 | 201 | PF00069 | 0.599 |
MOD_CK1_1 | 314 | 320 | PF00069 | 0.506 |
MOD_CK1_1 | 35 | 41 | PF00069 | 0.325 |
MOD_CK1_1 | 390 | 396 | PF00069 | 0.241 |
MOD_CK1_1 | 408 | 414 | PF00069 | 0.186 |
MOD_CK1_1 | 544 | 550 | PF00069 | 0.393 |
MOD_CK1_1 | 657 | 663 | PF00069 | 0.301 |
MOD_CK2_1 | 188 | 194 | PF00069 | 0.690 |
MOD_CK2_1 | 213 | 219 | PF00069 | 0.540 |
MOD_CK2_1 | 244 | 250 | PF00069 | 0.508 |
MOD_CK2_1 | 390 | 396 | PF00069 | 0.314 |
MOD_CK2_1 | 76 | 82 | PF00069 | 0.433 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.529 |
MOD_GlcNHglycan | 379 | 382 | PF01048 | 0.512 |
MOD_GlcNHglycan | 438 | 441 | PF01048 | 0.532 |
MOD_GlcNHglycan | 445 | 448 | PF01048 | 0.474 |
MOD_GlcNHglycan | 451 | 454 | PF01048 | 0.458 |
MOD_GlcNHglycan | 546 | 549 | PF01048 | 0.393 |
MOD_GlcNHglycan | 550 | 553 | PF01048 | 0.351 |
MOD_GlcNHglycan | 589 | 592 | PF01048 | 0.254 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.607 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.654 |
MOD_GSK3_1 | 311 | 318 | PF00069 | 0.683 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.454 |
MOD_GSK3_1 | 373 | 380 | PF00069 | 0.607 |
MOD_GSK3_1 | 387 | 394 | PF00069 | 0.506 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.248 |
MOD_GSK3_1 | 401 | 408 | PF00069 | 0.302 |
MOD_GSK3_1 | 544 | 551 | PF00069 | 0.353 |
MOD_GSK3_1 | 653 | 660 | PF00069 | 0.305 |
MOD_N-GLC_1 | 151 | 156 | PF02516 | 0.233 |
MOD_N-GLC_1 | 373 | 378 | PF02516 | 0.503 |
MOD_N-GLC_1 | 517 | 522 | PF02516 | 0.241 |
MOD_NEK2_1 | 15 | 20 | PF00069 | 0.194 |
MOD_NEK2_1 | 230 | 235 | PF00069 | 0.420 |
MOD_NEK2_1 | 275 | 280 | PF00069 | 0.249 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.503 |
MOD_NEK2_1 | 401 | 406 | PF00069 | 0.328 |
MOD_NEK2_1 | 449 | 454 | PF00069 | 0.415 |
MOD_NEK2_1 | 57 | 62 | PF00069 | 0.369 |
MOD_NEK2_1 | 608 | 613 | PF00069 | 0.430 |
MOD_NEK2_1 | 623 | 628 | PF00069 | 0.228 |
MOD_NEK2_1 | 646 | 651 | PF00069 | 0.460 |
MOD_NEK2_2 | 282 | 287 | PF00069 | 0.314 |
MOD_NEK2_2 | 288 | 293 | PF00069 | 0.314 |
MOD_NEK2_2 | 541 | 546 | PF00069 | 0.393 |
MOD_PIKK_1 | 594 | 600 | PF00454 | 0.241 |
MOD_PIKK_1 | 646 | 652 | PF00454 | 0.277 |
MOD_PKA_1 | 164 | 170 | PF00069 | 0.393 |
MOD_PKA_1 | 187 | 193 | PF00069 | 0.536 |
MOD_PKA_2 | 164 | 170 | PF00069 | 0.393 |
MOD_PKA_2 | 187 | 193 | PF00069 | 0.667 |
MOD_PKA_2 | 594 | 600 | PF00069 | 0.304 |
MOD_PKA_2 | 609 | 615 | PF00069 | 0.257 |
MOD_PKA_2 | 653 | 659 | PF00069 | 0.314 |
MOD_PKA_2 | 87 | 93 | PF00069 | 0.393 |
MOD_Plk_1 | 210 | 216 | PF00069 | 0.549 |
MOD_Plk_1 | 218 | 224 | PF00069 | 0.422 |
MOD_Plk_1 | 381 | 387 | PF00069 | 0.463 |
MOD_Plk_4 | 15 | 21 | PF00069 | 0.241 |
MOD_Plk_4 | 164 | 170 | PF00069 | 0.327 |
MOD_Plk_4 | 230 | 236 | PF00069 | 0.497 |
MOD_Plk_4 | 282 | 288 | PF00069 | 0.320 |
MOD_Plk_4 | 311 | 317 | PF00069 | 0.581 |
MOD_Plk_4 | 367 | 373 | PF00069 | 0.706 |
MOD_Plk_4 | 387 | 393 | PF00069 | 0.408 |
MOD_Plk_4 | 541 | 547 | PF00069 | 0.314 |
MOD_Plk_4 | 564 | 570 | PF00069 | 0.311 |
MOD_Plk_4 | 623 | 629 | PF00069 | 0.393 |
MOD_Plk_4 | 654 | 660 | PF00069 | 0.287 |
MOD_Plk_4 | 71 | 77 | PF00069 | 0.416 |
MOD_ProDKin_1 | 189 | 195 | PF00069 | 0.714 |
MOD_ProDKin_1 | 269 | 275 | PF00069 | 0.314 |
MOD_ProDKin_1 | 318 | 324 | PF00069 | 0.585 |
MOD_ProDKin_1 | 373 | 379 | PF00069 | 0.604 |
MOD_ProDKin_1 | 585 | 591 | PF00069 | 0.263 |
TRG_DiLeu_BaLyEn_6 | 11 | 16 | PF01217 | 0.334 |
TRG_DiLeu_BaLyEn_6 | 47 | 52 | PF01217 | 0.393 |
TRG_ENDOCYTIC_2 | 147 | 150 | PF00928 | 0.314 |
TRG_ENDOCYTIC_2 | 201 | 204 | PF00928 | 0.510 |
TRG_ENDOCYTIC_2 | 224 | 227 | PF00928 | 0.403 |
TRG_ENDOCYTIC_2 | 23 | 26 | PF00928 | 0.424 |
TRG_ENDOCYTIC_2 | 501 | 504 | PF00928 | 0.314 |
TRG_ENDOCYTIC_2 | 509 | 512 | PF00928 | 0.314 |
TRG_ENDOCYTIC_2 | 533 | 536 | PF00928 | 0.314 |
TRG_ENDOCYTIC_2 | 644 | 647 | PF00928 | 0.314 |
TRG_ER_diArg_1 | 163 | 165 | PF00400 | 0.314 |
TRG_ER_diArg_1 | 256 | 259 | PF00400 | 0.415 |
TRG_NES_CRM1_1 | 479 | 493 | PF08389 | 0.330 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDL0 | Leptomonas seymouri | 51% | 99% |
A0A3S7WV16 | Leishmania donovani | 75% | 97% |
A4HXW9 | Leishmania infantum | 75% | 97% |
E9ARN3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 73% | 100% |
Q4QDU6 | Leishmania major | 74% | 100% |