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. | yes | 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:0000506 | glycosylphosphatidylinositol-N-acetylglucosaminyltransferase (GPI-GnT) complex | 3 | 7 |
GO:0016020 | membrane | 2 | 7 |
GO:0032991 | protein-containing complex | 1 | 7 |
GO:0098796 | membrane protein complex | 2 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
GO:0140534 | endoplasmic reticulum protein-containing complex | 2 | 7 |
GO:1902494 | catalytic complex | 2 | 7 |
GO:1990234 | transferase complex | 3 | 7 |
Related structures:
AlphaFold database: A0A3S5H631
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:0003824 | catalytic activity | 1 | 2 |
GO:0016740 | transferase activity | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 486 | 490 | PF00656 | 0.621 |
CLV_MEL_PAP_1 | 249 | 255 | PF00089 | 0.323 |
CLV_NRD_NRD_1 | 4 | 6 | PF00675 | 0.453 |
CLV_NRD_NRD_1 | 62 | 64 | PF00675 | 0.447 |
CLV_PCSK_KEX2_1 | 26 | 28 | PF00082 | 0.486 |
CLV_PCSK_KEX2_1 | 366 | 368 | PF00082 | 0.347 |
CLV_PCSK_KEX2_1 | 4 | 6 | PF00082 | 0.453 |
CLV_PCSK_KEX2_1 | 62 | 64 | PF00082 | 0.447 |
CLV_PCSK_PC1ET2_1 | 26 | 28 | PF00082 | 0.478 |
CLV_PCSK_PC1ET2_1 | 366 | 368 | PF00082 | 0.347 |
CLV_PCSK_SKI1_1 | 224 | 228 | PF00082 | 0.410 |
CLV_PCSK_SKI1_1 | 332 | 336 | PF00082 | 0.655 |
CLV_PCSK_SKI1_1 | 453 | 457 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 460 | 464 | PF00082 | 0.370 |
DEG_APCC_DBOX_1 | 452 | 460 | PF00400 | 0.503 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.643 |
DEG_SPOP_SBC_1 | 315 | 319 | PF00917 | 0.469 |
DOC_CKS1_1 | 170 | 175 | PF01111 | 0.699 |
DOC_CKS1_1 | 503 | 508 | PF01111 | 0.671 |
DOC_CYCLIN_RxL_1 | 62 | 73 | PF00134 | 0.641 |
DOC_MAPK_gen_1 | 400 | 407 | PF00069 | 0.469 |
DOC_MAPK_MEF2A_6 | 400 | 409 | PF00069 | 0.469 |
DOC_MAPK_RevD_3 | 352 | 367 | PF00069 | 0.303 |
DOC_PP1_RVXF_1 | 222 | 228 | PF00149 | 0.646 |
DOC_PP1_RVXF_1 | 330 | 337 | PF00149 | 0.455 |
DOC_PP1_RVXF_1 | 436 | 443 | PF00149 | 0.469 |
DOC_PP2B_LxvP_1 | 174 | 177 | PF13499 | 0.690 |
DOC_USP7_MATH_1 | 103 | 107 | PF00917 | 0.652 |
DOC_USP7_MATH_1 | 281 | 285 | PF00917 | 0.481 |
DOC_USP7_MATH_1 | 3 | 7 | PF00917 | 0.665 |
DOC_USP7_MATH_1 | 315 | 319 | PF00917 | 0.489 |
DOC_USP7_MATH_1 | 32 | 36 | PF00917 | 0.709 |
DOC_USP7_MATH_1 | 45 | 49 | PF00917 | 0.779 |
DOC_USP7_MATH_1 | 52 | 56 | PF00917 | 0.732 |
DOC_USP7_MATH_2 | 467 | 473 | PF00917 | 0.648 |
DOC_WW_Pin1_4 | 166 | 171 | PF00397 | 0.757 |
DOC_WW_Pin1_4 | 177 | 182 | PF00397 | 0.710 |
DOC_WW_Pin1_4 | 197 | 202 | PF00397 | 0.663 |
DOC_WW_Pin1_4 | 27 | 32 | PF00397 | 0.656 |
DOC_WW_Pin1_4 | 296 | 301 | PF00397 | 0.502 |
DOC_WW_Pin1_4 | 342 | 347 | PF00397 | 0.261 |
DOC_WW_Pin1_4 | 502 | 507 | PF00397 | 0.685 |
DOC_WW_Pin1_4 | 92 | 97 | PF00397 | 0.800 |
LIG_14-3-3_CanoR_1 | 115 | 119 | PF00244 | 0.606 |
LIG_14-3-3_CanoR_1 | 18 | 23 | PF00244 | 0.639 |
LIG_14-3-3_CanoR_1 | 204 | 208 | PF00244 | 0.687 |
LIG_14-3-3_CanoR_1 | 252 | 256 | PF00244 | 0.383 |
LIG_14-3-3_CanoR_1 | 479 | 487 | PF00244 | 0.613 |
LIG_Actin_WH2_2 | 439 | 455 | PF00022 | 0.513 |
LIG_AP_GAE_1 | 495 | 501 | PF02883 | 0.695 |
LIG_APCC_ABBAyCdc20_2 | 460 | 466 | PF00400 | 0.533 |
LIG_EH1_1 | 402 | 410 | PF00400 | 0.516 |
LIG_eIF4E_1 | 376 | 382 | PF01652 | 0.541 |
LIG_EVH1_1 | 28 | 32 | PF00568 | 0.638 |
LIG_FHA_1 | 107 | 113 | PF00498 | 0.661 |
LIG_FHA_1 | 114 | 120 | PF00498 | 0.538 |
LIG_FHA_1 | 125 | 131 | PF00498 | 0.503 |
LIG_FHA_1 | 18 | 24 | PF00498 | 0.728 |
LIG_FHA_1 | 187 | 193 | PF00498 | 0.685 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.318 |
LIG_FHA_1 | 329 | 335 | PF00498 | 0.440 |
LIG_FHA_1 | 343 | 349 | PF00498 | 0.299 |
LIG_FHA_1 | 351 | 357 | PF00498 | 0.313 |
LIG_FHA_1 | 359 | 365 | PF00498 | 0.359 |
LIG_FHA_2 | 502 | 508 | PF00498 | 0.702 |
LIG_FHA_2 | 513 | 519 | PF00498 | 0.639 |
LIG_GBD_Chelix_1 | 364 | 372 | PF00786 | 0.417 |
LIG_LIR_Gen_1 | 268 | 277 | PF02991 | 0.453 |
LIG_LIR_Gen_1 | 360 | 368 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 268 | 272 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 360 | 365 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 391 | 396 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 398 | 404 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 417 | 422 | PF02991 | 0.469 |
LIG_MYND_1 | 78 | 82 | PF01753 | 0.687 |
LIG_MYND_3 | 272 | 276 | PF01753 | 0.359 |
LIG_NRBOX | 353 | 359 | PF00104 | 0.369 |
LIG_Pex14_1 | 223 | 227 | PF04695 | 0.647 |
LIG_Pex14_2 | 227 | 231 | PF04695 | 0.516 |
LIG_REV1ctd_RIR_1 | 417 | 423 | PF16727 | 0.469 |
LIG_RPA_C_Fungi | 58 | 70 | PF08784 | 0.553 |
LIG_SH2_NCK_1 | 339 | 343 | PF00017 | 0.506 |
LIG_SH2_STAP1 | 138 | 142 | PF00017 | 0.415 |
LIG_SH2_STAP1 | 188 | 192 | PF00017 | 0.521 |
LIG_SH2_STAT5 | 188 | 191 | PF00017 | 0.565 |
LIG_SH2_STAT5 | 339 | 342 | PF00017 | 0.510 |
LIG_SH2_STAT5 | 376 | 379 | PF00017 | 0.361 |
LIG_SH2_STAT5 | 441 | 444 | PF00017 | 0.477 |
LIG_SH3_1 | 26 | 32 | PF00018 | 0.547 |
LIG_SH3_3 | 167 | 173 | PF00018 | 0.749 |
LIG_SH3_3 | 26 | 32 | PF00018 | 0.576 |
LIG_SH3_3 | 437 | 443 | PF00018 | 0.304 |
LIG_SH3_3 | 448 | 454 | PF00018 | 0.367 |
LIG_SH3_3 | 500 | 506 | PF00018 | 0.580 |
LIG_SH3_3 | 6 | 12 | PF00018 | 0.580 |
LIG_SH3_3 | 75 | 81 | PF00018 | 0.671 |
LIG_SH3_3 | 90 | 96 | PF00018 | 0.756 |
LIG_SUMO_SIM_anti_2 | 349 | 356 | PF11976 | 0.349 |
LIG_SUMO_SIM_anti_2 | 378 | 384 | PF11976 | 0.369 |
LIG_SUMO_SIM_par_1 | 116 | 122 | PF11976 | 0.424 |
LIG_SUMO_SIM_par_1 | 234 | 240 | PF11976 | 0.303 |
LIG_SUMO_SIM_par_1 | 246 | 251 | PF11976 | 0.313 |
LIG_SUMO_SIM_par_1 | 353 | 361 | PF11976 | 0.406 |
LIG_SUMO_SIM_par_1 | 406 | 412 | PF11976 | 0.369 |
LIG_WRC_WIRS_1 | 192 | 197 | PF05994 | 0.532 |
LIG_WRC_WIRS_1 | 359 | 364 | PF05994 | 0.270 |
MOD_CDK_SPxxK_3 | 197 | 204 | PF00069 | 0.618 |
MOD_CK1_1 | 106 | 112 | PF00069 | 0.599 |
MOD_CK1_1 | 166 | 172 | PF00069 | 0.627 |
MOD_CK1_1 | 186 | 192 | PF00069 | 0.550 |
MOD_CK1_1 | 251 | 257 | PF00069 | 0.501 |
MOD_CK1_1 | 265 | 271 | PF00069 | 0.613 |
MOD_CK1_1 | 284 | 290 | PF00069 | 0.477 |
MOD_CK1_1 | 296 | 302 | PF00069 | 0.517 |
MOD_CK1_1 | 318 | 324 | PF00069 | 0.663 |
MOD_CK1_1 | 35 | 41 | PF00069 | 0.587 |
MOD_CK1_1 | 46 | 52 | PF00069 | 0.580 |
MOD_CK1_1 | 485 | 491 | PF00069 | 0.449 |
MOD_CK1_1 | 512 | 518 | PF00069 | 0.642 |
MOD_CK2_1 | 284 | 290 | PF00069 | 0.563 |
MOD_CK2_1 | 427 | 433 | PF00069 | 0.304 |
MOD_CK2_1 | 469 | 475 | PF00069 | 0.500 |
MOD_CK2_1 | 480 | 486 | PF00069 | 0.477 |
MOD_CK2_1 | 494 | 500 | PF00069 | 0.585 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.574 |
MOD_GlcNHglycan | 166 | 169 | PF01048 | 0.655 |
MOD_GlcNHglycan | 195 | 198 | PF01048 | 0.596 |
MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.537 |
MOD_GlcNHglycan | 283 | 286 | PF01048 | 0.674 |
MOD_GlcNHglycan | 295 | 298 | PF01048 | 0.566 |
MOD_GlcNHglycan | 301 | 304 | PF01048 | 0.606 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.644 |
MOD_GlcNHglycan | 368 | 371 | PF01048 | 0.383 |
MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.640 |
MOD_GlcNHglycan | 390 | 393 | PF01048 | 0.369 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.775 |
MOD_GlcNHglycan | 482 | 485 | PF01048 | 0.528 |
MOD_GlcNHglycan | 63 | 66 | PF01048 | 0.492 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.647 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.593 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.705 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.563 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.559 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.683 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.639 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.543 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.542 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.607 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.724 |
MOD_NEK2_1 | 195 | 200 | PF00069 | 0.604 |
MOD_NEK2_1 | 267 | 272 | PF00069 | 0.514 |
MOD_NEK2_1 | 335 | 340 | PF00069 | 0.592 |
MOD_NEK2_1 | 348 | 353 | PF00069 | 0.272 |
MOD_NEK2_1 | 357 | 362 | PF00069 | 0.314 |
MOD_NEK2_1 | 388 | 393 | PF00069 | 0.304 |
MOD_NEK2_1 | 409 | 414 | PF00069 | 0.304 |
MOD_NEK2_1 | 426 | 431 | PF00069 | 0.304 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.536 |
MOD_PIKK_1 | 337 | 343 | PF00454 | 0.521 |
MOD_PKA_1 | 366 | 372 | PF00069 | 0.476 |
MOD_PKA_2 | 114 | 120 | PF00069 | 0.508 |
MOD_PKA_2 | 17 | 23 | PF00069 | 0.476 |
MOD_PKA_2 | 203 | 209 | PF00069 | 0.609 |
MOD_PKA_2 | 251 | 257 | PF00069 | 0.519 |
MOD_PKA_2 | 3 | 9 | PF00069 | 0.549 |
MOD_PKA_2 | 366 | 372 | PF00069 | 0.476 |
MOD_PKA_2 | 61 | 67 | PF00069 | 0.551 |
MOD_Plk_1 | 211 | 217 | PF00069 | 0.583 |
MOD_Plk_1 | 348 | 354 | PF00069 | 0.331 |
MOD_Plk_1 | 494 | 500 | PF00069 | 0.615 |
MOD_Plk_2-3 | 469 | 475 | PF00069 | 0.500 |
MOD_Plk_2-3 | 491 | 497 | PF00069 | 0.493 |
MOD_Plk_4 | 114 | 120 | PF00069 | 0.443 |
MOD_Plk_4 | 18 | 24 | PF00069 | 0.617 |
MOD_Plk_4 | 251 | 257 | PF00069 | 0.592 |
MOD_Plk_4 | 321 | 327 | PF00069 | 0.581 |
MOD_Plk_4 | 350 | 356 | PF00069 | 0.404 |
MOD_Plk_4 | 358 | 364 | PF00069 | 0.369 |
MOD_ProDKin_1 | 166 | 172 | PF00069 | 0.705 |
MOD_ProDKin_1 | 177 | 183 | PF00069 | 0.639 |
MOD_ProDKin_1 | 197 | 203 | PF00069 | 0.578 |
MOD_ProDKin_1 | 27 | 33 | PF00069 | 0.569 |
MOD_ProDKin_1 | 296 | 302 | PF00069 | 0.632 |
MOD_ProDKin_1 | 342 | 348 | PF00069 | 0.292 |
MOD_ProDKin_1 | 502 | 508 | PF00069 | 0.609 |
MOD_ProDKin_1 | 92 | 98 | PF00069 | 0.763 |
MOD_SUMO_rev_2 | 429 | 436 | PF00179 | 0.369 |
TRG_DiLeu_BaEn_4 | 468 | 474 | PF01217 | 0.493 |
TRG_ENDOCYTIC_2 | 393 | 396 | PF00928 | 0.304 |
TRG_ENDOCYTIC_2 | 401 | 404 | PF00928 | 0.304 |
TRG_ENDOCYTIC_2 | 422 | 425 | PF00928 | 0.304 |
TRG_ER_diArg_1 | 3 | 5 | PF00400 | 0.593 |
TRG_NES_CRM1_1 | 406 | 417 | PF08389 | 0.304 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I406 | Leptomonas seymouri | 50% | 100% |
A4H582 | Leishmania braziliensis | 68% | 99% |
A4HTG6 | Leishmania infantum | 99% | 100% |
E9AM94 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 99% |
Q4QIF4 | Leishmania major | 89% | 100% |