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: E9ARN3
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 | 0.643 |
CLV_C14_Caspase3-7 | 354 | 358 | PF00656 | 0.679 |
CLV_NRD_NRD_1 | 164 | 166 | PF00675 | 0.280 |
CLV_NRD_NRD_1 | 198 | 200 | PF00675 | 0.525 |
CLV_NRD_NRD_1 | 259 | 261 | PF00675 | 0.289 |
CLV_NRD_NRD_1 | 594 | 596 | PF00675 | 0.296 |
CLV_PCSK_FUR_1 | 257 | 261 | PF00082 | 0.301 |
CLV_PCSK_KEX2_1 | 164 | 166 | PF00082 | 0.271 |
CLV_PCSK_KEX2_1 | 257 | 259 | PF00082 | 0.361 |
CLV_PCSK_KEX2_1 | 522 | 524 | PF00082 | 0.432 |
CLV_PCSK_KEX2_1 | 594 | 596 | PF00082 | 0.296 |
CLV_PCSK_PC1ET2_1 | 522 | 524 | PF00082 | 0.400 |
CLV_PCSK_SKI1_1 | 164 | 168 | PF00082 | 0.319 |
CLV_PCSK_SKI1_1 | 200 | 204 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 381 | 385 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 50 | 54 | PF00082 | 0.374 |
CLV_PCSK_SKI1_1 | 511 | 515 | PF00082 | 0.471 |
CLV_PCSK_SKI1_1 | 635 | 639 | PF00082 | 0.443 |
DEG_APCC_DBOX_1 | 181 | 189 | PF00400 | 0.557 |
DEG_APCC_DBOX_1 | 49 | 57 | PF00400 | 0.306 |
DEG_MDM2_SWIB_1 | 662 | 669 | PF02201 | 0.204 |
DEG_ODPH_VHL_1 | 134 | 146 | PF01847 | 0.233 |
DEG_SCF_FBW7_1 | 373 | 380 | PF00400 | 0.604 |
DOC_AGCK_PIF_1 | 546 | 551 | PF00069 | 0.281 |
DOC_CDC14_PxL_1 | 117 | 125 | PF14671 | 0.271 |
DOC_CKS1_1 | 190 | 195 | PF01111 | 0.654 |
DOC_CKS1_1 | 270 | 275 | PF01111 | 0.306 |
DOC_CYCLIN_yCln2_LP_2 | 338 | 341 | PF00134 | 0.669 |
DOC_CYCLIN_yCln2_LP_2 | 420 | 426 | PF00134 | 0.374 |
DOC_CYCLIN_yCln2_LP_2 | 559 | 565 | PF00134 | 0.306 |
DOC_MAPK_gen_1 | 164 | 171 | PF00069 | 0.479 |
DOC_MAPK_gen_1 | 199 | 208 | PF00069 | 0.611 |
DOC_MAPK_gen_1 | 461 | 469 | PF00069 | 0.578 |
DOC_MAPK_gen_1 | 538 | 545 | PF00069 | 0.304 |
DOC_MAPK_gen_1 | 594 | 603 | PF00069 | 0.485 |
DOC_MAPK_MEF2A_6 | 50 | 57 | PF00069 | 0.204 |
DOC_MAPK_MEF2A_6 | 594 | 603 | PF00069 | 0.409 |
DOC_MAPK_NFAT4_5 | 50 | 58 | PF00069 | 0.204 |
DOC_PP1_RVXF_1 | 12 | 19 | PF00149 | 0.320 |
DOC_PP2B_LxvP_1 | 235 | 238 | PF13499 | 0.628 |
DOC_PP2B_LxvP_1 | 338 | 341 | PF13499 | 0.707 |
DOC_PP2B_LxvP_1 | 474 | 477 | PF13499 | 0.658 |
DOC_PP2B_LxvP_1 | 559 | 562 | PF13499 | 0.352 |
DOC_PP4_FxxP_1 | 171 | 174 | PF00568 | 0.521 |
DOC_PP4_FxxP_1 | 68 | 71 | PF00568 | 0.523 |
DOC_USP7_MATH_1 | 213 | 217 | PF00917 | 0.526 |
DOC_USP7_MATH_1 | 317 | 321 | PF00917 | 0.559 |
DOC_USP7_MATH_1 | 332 | 336 | PF00917 | 0.760 |
DOC_USP7_MATH_1 | 377 | 381 | PF00917 | 0.596 |
DOC_USP7_MATH_1 | 436 | 440 | PF00917 | 0.616 |
DOC_USP7_MATH_1 | 443 | 447 | PF00917 | 0.565 |
DOC_USP7_MATH_1 | 607 | 611 | PF00917 | 0.309 |
DOC_WW_Pin1_4 | 186 | 191 | PF00397 | 0.689 |
DOC_WW_Pin1_4 | 269 | 274 | PF00397 | 0.306 |
DOC_WW_Pin1_4 | 318 | 323 | PF00397 | 0.644 |
DOC_WW_Pin1_4 | 373 | 378 | PF00397 | 0.649 |
DOC_WW_Pin1_4 | 637 | 642 | PF00397 | 0.282 |
LIG_14-3-3_CanoR_1 | 178 | 185 | PF00244 | 0.623 |
LIG_14-3-3_CanoR_1 | 311 | 316 | PF00244 | 0.663 |
LIG_14-3-3_CanoR_1 | 381 | 386 | PF00244 | 0.614 |
LIG_14-3-3_CanoR_1 | 464 | 468 | PF00244 | 0.691 |
LIG_14-3-3_CanoR_1 | 635 | 641 | PF00244 | 0.330 |
LIG_14-3-3_CanoR_1 | 88 | 92 | PF00244 | 0.519 |
LIG_APCC_ABBA_1 | 20 | 25 | PF00400 | 0.482 |
LIG_APCC_ABBA_1 | 279 | 284 | PF00400 | 0.321 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.597 |
LIG_BRCT_BRCA1_1 | 410 | 414 | PF00533 | 0.297 |
LIG_CaM_NSCaTE_8 | 541 | 548 | PF13499 | 0.319 |
LIG_DLG_GKlike_1 | 311 | 319 | PF00625 | 0.622 |
LIG_eIF4E_1 | 540 | 546 | PF01652 | 0.281 |
LIG_EVH1_1 | 339 | 343 | PF00568 | 0.582 |
LIG_FHA_1 | 129 | 135 | PF00498 | 0.293 |
LIG_FHA_1 | 190 | 196 | PF00498 | 0.662 |
LIG_FHA_1 | 229 | 235 | PF00498 | 0.613 |
LIG_FHA_1 | 276 | 282 | PF00498 | 0.293 |
LIG_FHA_1 | 38 | 44 | PF00498 | 0.319 |
LIG_FHA_1 | 464 | 470 | PF00498 | 0.666 |
LIG_FHA_1 | 638 | 644 | PF00498 | 0.433 |
LIG_FHA_2 | 231 | 237 | PF00498 | 0.573 |
LIG_FHA_2 | 245 | 251 | PF00498 | 0.587 |
LIG_FHA_2 | 34 | 40 | PF00498 | 0.367 |
LIG_FHA_2 | 77 | 83 | PF00498 | 0.541 |
LIG_GBD_Chelix_1 | 397 | 405 | PF00786 | 0.374 |
LIG_GBD_Chelix_1 | 48 | 56 | PF00786 | 0.374 |
LIG_LIR_Apic_2 | 170 | 174 | PF02991 | 0.471 |
LIG_LIR_Gen_1 | 25 | 34 | PF02991 | 0.342 |
LIG_LIR_Gen_1 | 384 | 392 | PF02991 | 0.517 |
LIG_LIR_Gen_1 | 550 | 559 | PF02991 | 0.227 |
LIG_LIR_Gen_1 | 660 | 669 | PF02991 | 0.469 |
LIG_LIR_Gen_1 | 86 | 96 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 25 | 31 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 384 | 390 | PF02991 | 0.528 |
LIG_LIR_Nem_3 | 544 | 549 | PF02991 | 0.313 |
LIG_LIR_Nem_3 | 550 | 554 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 596 | 601 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 660 | 665 | PF02991 | 0.493 |
LIG_LIR_Nem_3 | 86 | 92 | PF02991 | 0.471 |
LIG_LYPXL_S_1 | 532 | 536 | PF13949 | 0.471 |
LIG_LYPXL_yS_3 | 533 | 536 | PF13949 | 0.271 |
LIG_MYND_1 | 472 | 476 | PF01753 | 0.662 |
LIG_NRBOX | 50 | 56 | PF00104 | 0.204 |
LIG_NRBOX | 616 | 622 | PF00104 | 0.282 |
LIG_NRBOX | 642 | 648 | PF00104 | 0.306 |
LIG_PCNA_PIPBox_1 | 309 | 318 | PF02747 | 0.665 |
LIG_Pex14_1 | 387 | 391 | PF04695 | 0.584 |
LIG_Pex14_2 | 662 | 666 | PF04695 | 0.204 |
LIG_RPA_C_Fungi | 254 | 266 | PF08784 | 0.374 |
LIG_SH2_CRK | 106 | 110 | PF00017 | 0.316 |
LIG_SH2_GRB2like | 110 | 113 | PF00017 | 0.203 |
LIG_SH2_NCK_1 | 201 | 205 | PF00017 | 0.511 |
LIG_SH2_NCK_1 | 23 | 27 | PF00017 | 0.523 |
LIG_SH2_PTP2 | 147 | 150 | PF00017 | 0.374 |
LIG_SH2_SRC | 84 | 87 | PF00017 | 0.473 |
LIG_SH2_STAP1 | 106 | 110 | PF00017 | 0.284 |
LIG_SH2_STAP1 | 282 | 286 | PF00017 | 0.335 |
LIG_SH2_STAT3 | 110 | 113 | PF00017 | 0.282 |
LIG_SH2_STAT5 | 108 | 111 | PF00017 | 0.325 |
LIG_SH2_STAT5 | 129 | 132 | PF00017 | 0.217 |
LIG_SH2_STAT5 | 147 | 150 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 23 | 26 | PF00017 | 0.581 |
LIG_SH2_STAT5 | 282 | 285 | PF00017 | 0.339 |
LIG_SH2_STAT5 | 296 | 299 | PF00017 | 0.306 |
LIG_SH2_STAT5 | 315 | 318 | PF00017 | 0.521 |
LIG_SH2_STAT5 | 33 | 36 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 501 | 504 | PF00017 | 0.329 |
LIG_SH2_STAT5 | 549 | 552 | PF00017 | 0.306 |
LIG_SH2_STAT6 | 508 | 512 | PF00017 | 0.257 |
LIG_SH3_1 | 187 | 193 | PF00018 | 0.562 |
LIG_SH3_1 | 337 | 343 | PF00018 | 0.635 |
LIG_SH3_3 | 115 | 121 | PF00018 | 0.308 |
LIG_SH3_3 | 16 | 22 | PF00018 | 0.401 |
LIG_SH3_3 | 187 | 193 | PF00018 | 0.562 |
LIG_SH3_3 | 316 | 322 | PF00018 | 0.491 |
LIG_SH3_3 | 337 | 343 | PF00018 | 0.635 |
LIG_SH3_3 | 425 | 431 | PF00018 | 0.410 |
LIG_SH3_3 | 466 | 472 | PF00018 | 0.575 |
LIG_SH3_3 | 494 | 500 | PF00018 | 0.377 |
LIG_SUMO_SIM_par_1 | 277 | 285 | PF11976 | 0.244 |
LIG_SUMO_SIM_par_1 | 488 | 493 | PF11976 | 0.306 |
LIG_SUMO_SIM_par_1 | 561 | 567 | PF11976 | 0.374 |
LIG_SxIP_EBH_1 | 362 | 371 | PF03271 | 0.611 |
LIG_TRAF2_1 | 79 | 82 | PF00917 | 0.401 |
LIG_TRFH_1 | 18 | 22 | PF08558 | 0.320 |
LIG_ULM_U2AF65_1 | 594 | 599 | PF00076 | 0.320 |
LIG_Vh1_VBS_1 | 390 | 408 | PF01044 | 0.204 |
LIG_WRC_WIRS_1 | 168 | 173 | PF05994 | 0.306 |
MOD_CK1_1 | 186 | 192 | PF00069 | 0.558 |
MOD_CK1_1 | 285 | 291 | PF00069 | 0.320 |
MOD_CK1_1 | 318 | 324 | PF00069 | 0.545 |
MOD_CK1_1 | 446 | 452 | PF00069 | 0.363 |
MOD_CK1_1 | 544 | 550 | PF00069 | 0.374 |
MOD_CK1_1 | 653 | 659 | PF00069 | 0.324 |
MOD_CK1_1 | 660 | 666 | PF00069 | 0.288 |
MOD_CK2_1 | 188 | 194 | PF00069 | 0.632 |
MOD_CK2_1 | 213 | 219 | PF00069 | 0.618 |
MOD_CK2_1 | 244 | 250 | PF00069 | 0.642 |
MOD_CK2_1 | 390 | 396 | PF00069 | 0.306 |
MOD_CK2_1 | 76 | 82 | PF00069 | 0.400 |
MOD_GlcNHglycan | 323 | 326 | PF01048 | 0.574 |
MOD_GlcNHglycan | 332 | 335 | PF01048 | 0.564 |
MOD_GlcNHglycan | 438 | 441 | PF01048 | 0.524 |
MOD_GlcNHglycan | 445 | 448 | PF01048 | 0.458 |
MOD_GlcNHglycan | 451 | 454 | PF01048 | 0.448 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.288 |
MOD_GlcNHglycan | 518 | 522 | PF01048 | 0.215 |
MOD_GlcNHglycan | 546 | 549 | PF01048 | 0.374 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.693 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.385 |
MOD_GSK3_1 | 311 | 318 | PF00069 | 0.610 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.567 |
MOD_GSK3_1 | 367 | 374 | PF00069 | 0.697 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.563 |
MOD_GSK3_1 | 408 | 415 | PF00069 | 0.355 |
MOD_GSK3_1 | 650 | 657 | PF00069 | 0.318 |
MOD_N-GLC_1 | 330 | 335 | PF02516 | 0.466 |
MOD_NEK2_1 | 195 | 200 | PF00069 | 0.470 |
MOD_NEK2_1 | 230 | 235 | PF00069 | 0.444 |
MOD_NEK2_1 | 275 | 280 | PF00069 | 0.277 |
MOD_NEK2_1 | 390 | 395 | PF00069 | 0.318 |
MOD_NEK2_1 | 405 | 410 | PF00069 | 0.335 |
MOD_NEK2_1 | 57 | 62 | PF00069 | 0.357 |
MOD_NEK2_1 | 608 | 613 | PF00069 | 0.438 |
MOD_NEK2_1 | 623 | 628 | PF00069 | 0.245 |
MOD_NEK2_1 | 636 | 641 | PF00069 | 0.321 |
MOD_NEK2_2 | 282 | 287 | PF00069 | 0.306 |
MOD_NEK2_2 | 541 | 546 | PF00069 | 0.374 |
MOD_PKA_1 | 164 | 170 | PF00069 | 0.374 |
MOD_PKA_2 | 164 | 170 | PF00069 | 0.374 |
MOD_PKA_2 | 177 | 183 | PF00069 | 0.360 |
MOD_PKA_2 | 228 | 234 | PF00069 | 0.454 |
MOD_PKA_2 | 463 | 469 | PF00069 | 0.501 |
MOD_PKA_2 | 593 | 599 | PF00069 | 0.317 |
MOD_PKA_2 | 653 | 659 | PF00069 | 0.347 |
MOD_PKA_2 | 87 | 93 | PF00069 | 0.374 |
MOD_Plk_1 | 218 | 224 | PF00069 | 0.434 |
MOD_Plk_4 | 104 | 110 | PF00069 | 0.264 |
MOD_Plk_4 | 164 | 170 | PF00069 | 0.371 |
MOD_Plk_4 | 230 | 236 | PF00069 | 0.555 |
MOD_Plk_4 | 244 | 250 | PF00069 | 0.545 |
MOD_Plk_4 | 282 | 288 | PF00069 | 0.317 |
MOD_Plk_4 | 311 | 317 | PF00069 | 0.588 |
MOD_Plk_4 | 367 | 373 | PF00069 | 0.615 |
MOD_Plk_4 | 541 | 547 | PF00069 | 0.306 |
MOD_Plk_4 | 623 | 629 | PF00069 | 0.374 |
MOD_Plk_4 | 71 | 77 | PF00069 | 0.384 |
MOD_ProDKin_1 | 186 | 192 | PF00069 | 0.610 |
MOD_ProDKin_1 | 269 | 275 | PF00069 | 0.306 |
MOD_ProDKin_1 | 318 | 324 | PF00069 | 0.551 |
MOD_ProDKin_1 | 373 | 379 | PF00069 | 0.548 |
MOD_ProDKin_1 | 637 | 643 | PF00069 | 0.282 |
MOD_SUMO_for_1 | 385 | 388 | PF00179 | 0.501 |
MOD_SUMO_for_1 | 521 | 524 | PF00179 | 0.204 |
TRG_DiLeu_BaLyEn_6 | 11 | 16 | PF01217 | 0.320 |
TRG_DiLeu_BaLyEn_6 | 334 | 339 | PF01217 | 0.466 |
TRG_DiLeu_BaLyEn_6 | 47 | 52 | PF01217 | 0.374 |
TRG_ENDOCYTIC_2 | 106 | 109 | PF00928 | 0.286 |
TRG_ENDOCYTIC_2 | 147 | 150 | PF00928 | 0.306 |
TRG_ENDOCYTIC_2 | 224 | 227 | PF00928 | 0.424 |
TRG_ENDOCYTIC_2 | 501 | 504 | PF00928 | 0.306 |
TRG_ENDOCYTIC_2 | 509 | 512 | PF00928 | 0.306 |
TRG_ENDOCYTIC_2 | 533 | 536 | PF00928 | 0.306 |
TRG_ENDOCYTIC_2 | 540 | 543 | PF00928 | 0.306 |
TRG_ENDOCYTIC_2 | 644 | 647 | PF00928 | 0.306 |
TRG_ER_diArg_1 | 163 | 165 | PF00400 | 0.306 |
TRG_ER_diArg_1 | 256 | 259 | PF00400 | 0.441 |
TRG_ER_diArg_1 | 362 | 365 | PF00400 | 0.587 |
TRG_ER_diArg_1 | 593 | 595 | PF00400 | 0.315 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDL0 | Leptomonas seymouri | 51% | 99% |
A0A3S7WV16 | Leishmania donovani | 88% | 97% |
A4H9K3 | Leishmania braziliensis | 73% | 100% |
A4HXW9 | Leishmania infantum | 87% | 97% |
Q4QDU6 | Leishmania major | 86% | 100% |