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: 1, no: 5 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
Related structures:
AlphaFold database: A4HMB6
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 7 |
GO:0006644 | phospholipid metabolic process | 4 | 7 |
GO:0006793 | phosphorus metabolic process | 3 | 7 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 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:0009987 | cellular process | 1 | 7 |
GO:0019637 | organophosphate metabolic process | 3 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0044255 | cellular lipid metabolic process | 3 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:0090407 | organophosphate biosynthetic process | 4 | 7 |
GO:1901576 | organic substance biosynthetic process | 3 | 7 |
GO:0006650 | glycerophospholipid metabolic process | 5 | 1 |
GO:0006656 | phosphatidylcholine biosynthetic process | 5 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0044249 | cellular biosynthetic process | 3 | 1 |
GO:0045017 | glycerolipid biosynthetic process | 4 | 1 |
GO:0046470 | phosphatidylcholine metabolic process | 4 | 1 |
GO:0046474 | glycerophospholipid biosynthetic process | 5 | 1 |
GO:0046486 | glycerolipid metabolic process | 4 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0016740 | transferase activity | 2 | 7 |
GO:0016746 | acyltransferase activity | 3 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 220 | 224 | PF00656 | 0.372 |
CLV_C14_Caspase3-7 | 255 | 259 | PF00656 | 0.375 |
CLV_C14_Caspase3-7 | 380 | 384 | PF00656 | 0.580 |
CLV_NRD_NRD_1 | 216 | 218 | PF00675 | 0.634 |
CLV_NRD_NRD_1 | 321 | 323 | PF00675 | 0.671 |
CLV_NRD_NRD_1 | 351 | 353 | PF00675 | 0.417 |
CLV_NRD_NRD_1 | 357 | 359 | PF00675 | 0.446 |
CLV_NRD_NRD_1 | 370 | 372 | PF00675 | 0.461 |
CLV_NRD_NRD_1 | 418 | 420 | PF00675 | 0.507 |
CLV_PCSK_FUR_1 | 355 | 359 | PF00082 | 0.323 |
CLV_PCSK_KEX2_1 | 216 | 218 | PF00082 | 0.642 |
CLV_PCSK_KEX2_1 | 321 | 323 | PF00082 | 0.671 |
CLV_PCSK_KEX2_1 | 351 | 353 | PF00082 | 0.417 |
CLV_PCSK_KEX2_1 | 357 | 359 | PF00082 | 0.446 |
CLV_PCSK_KEX2_1 | 361 | 363 | PF00082 | 0.446 |
CLV_PCSK_PC1ET2_1 | 361 | 363 | PF00082 | 0.519 |
CLV_PCSK_PC7_1 | 357 | 363 | PF00082 | 0.358 |
CLV_PCSK_SKI1_1 | 180 | 184 | PF00082 | 0.594 |
CLV_PCSK_SKI1_1 | 210 | 214 | PF00082 | 0.591 |
CLV_PCSK_SKI1_1 | 322 | 326 | PF00082 | 0.654 |
CLV_PCSK_SKI1_1 | 362 | 366 | PF00082 | 0.507 |
CLV_PCSK_SKI1_1 | 371 | 375 | PF00082 | 0.531 |
CLV_PCSK_SKI1_1 | 420 | 424 | PF00082 | 0.379 |
CLV_PCSK_SKI1_1 | 425 | 429 | PF00082 | 0.357 |
CLV_PCSK_SKI1_1 | 494 | 498 | PF00082 | 0.308 |
CLV_PCSK_SKI1_1 | 525 | 529 | PF00082 | 0.352 |
DOC_CYCLIN_yCln2_LP_2 | 386 | 392 | PF00134 | 0.582 |
DOC_MAPK_gen_1 | 124 | 133 | PF00069 | 0.523 |
DOC_MAPK_MEF2A_6 | 110 | 119 | PF00069 | 0.390 |
DOC_MAPK_MEF2A_6 | 127 | 135 | PF00069 | 0.419 |
DOC_PP1_RVXF_1 | 329 | 335 | PF00149 | 0.513 |
DOC_PP2B_LxvP_1 | 117 | 120 | PF13499 | 0.545 |
DOC_PP2B_LxvP_1 | 238 | 241 | PF13499 | 0.342 |
DOC_PP2B_PxIxI_1 | 457 | 463 | PF00149 | 0.397 |
DOC_USP7_MATH_1 | 241 | 245 | PF00917 | 0.381 |
DOC_USP7_MATH_1 | 391 | 395 | PF00917 | 0.742 |
DOC_USP7_UBL2_3 | 361 | 365 | PF12436 | 0.654 |
DOC_USP7_UBL2_3 | 494 | 498 | PF12436 | 0.689 |
DOC_USP7_UBL2_3 | 525 | 529 | PF12436 | 0.552 |
DOC_USP7_UBL2_3 | 56 | 60 | PF12436 | 0.327 |
DOC_WW_Pin1_4 | 104 | 109 | PF00397 | 0.463 |
DOC_WW_Pin1_4 | 397 | 402 | PF00397 | 0.696 |
LIG_14-3-3_CanoR_1 | 190 | 198 | PF00244 | 0.372 |
LIG_14-3-3_CanoR_1 | 210 | 219 | PF00244 | 0.249 |
LIG_14-3-3_CanoR_1 | 280 | 286 | PF00244 | 0.572 |
LIG_14-3-3_CanoR_1 | 321 | 327 | PF00244 | 0.396 |
LIG_14-3-3_CanoR_1 | 371 | 379 | PF00244 | 0.562 |
LIG_14-3-3_CanoR_1 | 404 | 409 | PF00244 | 0.611 |
LIG_14-3-3_CanoR_1 | 434 | 440 | PF00244 | 0.605 |
LIG_Actin_WH2_2 | 282 | 299 | PF00022 | 0.536 |
LIG_APCC_ABBA_1 | 427 | 432 | PF00400 | 0.683 |
LIG_BRCT_BRCA1_1 | 282 | 286 | PF00533 | 0.380 |
LIG_EH1_1 | 8 | 16 | PF00400 | 0.302 |
LIG_eIF4E_1 | 9 | 15 | PF01652 | 0.290 |
LIG_FHA_1 | 266 | 272 | PF00498 | 0.532 |
LIG_FHA_1 | 302 | 308 | PF00498 | 0.521 |
LIG_FHA_1 | 380 | 386 | PF00498 | 0.606 |
LIG_FHA_1 | 442 | 448 | PF00498 | 0.559 |
LIG_FHA_1 | 526 | 532 | PF00498 | 0.647 |
LIG_FHA_2 | 148 | 154 | PF00498 | 0.634 |
LIG_FHA_2 | 344 | 350 | PF00498 | 0.483 |
LIG_FHA_2 | 378 | 384 | PF00498 | 0.727 |
LIG_LIR_Apic_2 | 98 | 102 | PF02991 | 0.580 |
LIG_LIR_Gen_1 | 112 | 122 | PF02991 | 0.513 |
LIG_LIR_Gen_1 | 136 | 145 | PF02991 | 0.499 |
LIG_LIR_Gen_1 | 156 | 166 | PF02991 | 0.619 |
LIG_LIR_Gen_1 | 187 | 196 | PF02991 | 0.362 |
LIG_LIR_Gen_1 | 283 | 291 | PF02991 | 0.549 |
LIG_LIR_Gen_1 | 35 | 44 | PF02991 | 0.411 |
LIG_LIR_Gen_1 | 370 | 379 | PF02991 | 0.662 |
LIG_LIR_Gen_1 | 406 | 416 | PF02991 | 0.535 |
LIG_LIR_Nem_3 | 112 | 117 | PF02991 | 0.499 |
LIG_LIR_Nem_3 | 129 | 135 | PF02991 | 0.375 |
LIG_LIR_Nem_3 | 136 | 140 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 156 | 161 | PF02991 | 0.589 |
LIG_LIR_Nem_3 | 168 | 172 | PF02991 | 0.333 |
LIG_LIR_Nem_3 | 18 | 24 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 192 | 198 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 283 | 289 | PF02991 | 0.555 |
LIG_LIR_Nem_3 | 325 | 329 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 35 | 39 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 370 | 376 | PF02991 | 0.660 |
LIG_LIR_Nem_3 | 454 | 460 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 469 | 474 | PF02991 | 0.330 |
LIG_LIR_Nem_3 | 71 | 75 | PF02991 | 0.455 |
LIG_LYPXL_yS_3 | 457 | 460 | PF13949 | 0.411 |
LIG_NRBOX | 44 | 50 | PF00104 | 0.261 |
LIG_PCNA_yPIPBox_3 | 236 | 246 | PF02747 | 0.517 |
LIG_PCNA_yPIPBox_3 | 41 | 51 | PF02747 | 0.513 |
LIG_Pex14_1 | 340 | 344 | PF04695 | 0.411 |
LIG_Pex14_2 | 158 | 162 | PF04695 | 0.411 |
LIG_Pex14_2 | 29 | 33 | PF04695 | 0.438 |
LIG_Pex14_2 | 343 | 347 | PF04695 | 0.482 |
LIG_Pex14_2 | 426 | 430 | PF04695 | 0.605 |
LIG_PTB_Apo_2 | 93 | 100 | PF02174 | 0.409 |
LIG_PTB_Phospho_1 | 93 | 99 | PF10480 | 0.407 |
LIG_SH2_CRK | 19 | 23 | PF00017 | 0.261 |
LIG_SH2_CRK | 313 | 317 | PF00017 | 0.509 |
LIG_SH2_CRK | 326 | 330 | PF00017 | 0.300 |
LIG_SH2_NCK_1 | 228 | 232 | PF00017 | 0.505 |
LIG_SH2_SRC | 132 | 135 | PF00017 | 0.513 |
LIG_SH2_SRC | 228 | 231 | PF00017 | 0.507 |
LIG_SH2_STAP1 | 408 | 412 | PF00017 | 0.538 |
LIG_SH2_STAP1 | 466 | 470 | PF00017 | 0.312 |
LIG_SH2_STAT3 | 24 | 27 | PF00017 | 0.619 |
LIG_SH2_STAT5 | 132 | 135 | PF00017 | 0.472 |
LIG_SH2_STAT5 | 144 | 147 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 195 | 198 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 21 | 24 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 31 | 34 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 36 | 39 | PF00017 | 0.336 |
LIG_SH2_STAT5 | 408 | 411 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 466 | 469 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 9 | 12 | PF00017 | 0.411 |
LIG_SH3_3 | 128 | 134 | PF00018 | 0.419 |
LIG_TYR_ITIM | 324 | 329 | PF00017 | 0.380 |
LIG_UBA3_1 | 13 | 20 | PF00899 | 0.404 |
LIG_UBA3_1 | 48 | 56 | PF00899 | 0.554 |
LIG_WRC_WIRS_1 | 155 | 160 | PF05994 | 0.619 |
LIG_WRC_WIRS_1 | 185 | 190 | PF05994 | 0.346 |
LIG_WRC_WIRS_1 | 344 | 349 | PF05994 | 0.476 |
MOD_CDK_SPxK_1 | 104 | 110 | PF00069 | 0.503 |
MOD_CDK_SPxxK_3 | 397 | 404 | PF00069 | 0.663 |
MOD_CK1_1 | 248 | 254 | PF00069 | 0.443 |
MOD_CK1_1 | 257 | 263 | PF00069 | 0.394 |
MOD_CK1_1 | 284 | 290 | PF00069 | 0.522 |
MOD_CK1_1 | 64 | 70 | PF00069 | 0.381 |
MOD_CK2_1 | 147 | 153 | PF00069 | 0.638 |
MOD_CK2_1 | 343 | 349 | PF00069 | 0.479 |
MOD_CK2_1 | 397 | 403 | PF00069 | 0.671 |
MOD_CK2_1 | 508 | 514 | PF00069 | 0.526 |
MOD_Cter_Amidation | 417 | 420 | PF01082 | 0.512 |
MOD_GlcNHglycan | 213 | 216 | PF01048 | 0.592 |
MOD_GlcNHglycan | 258 | 262 | PF01048 | 0.628 |
MOD_GlcNHglycan | 41 | 44 | PF01048 | 0.261 |
MOD_GlcNHglycan | 468 | 471 | PF01048 | 0.572 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.628 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.386 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.449 |
MOD_GSK3_1 | 430 | 437 | PF00069 | 0.558 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.351 |
MOD_N-GLC_1 | 265 | 270 | PF02516 | 0.704 |
MOD_N-GLC_1 | 80 | 85 | PF02516 | 0.723 |
MOD_N-GLC_1 | 95 | 100 | PF02516 | 0.617 |
MOD_NEK2_1 | 165 | 170 | PF00069 | 0.460 |
MOD_NEK2_1 | 211 | 216 | PF00069 | 0.477 |
MOD_NEK2_1 | 252 | 257 | PF00069 | 0.500 |
MOD_NEK2_1 | 281 | 286 | PF00069 | 0.541 |
MOD_NEK2_1 | 296 | 301 | PF00069 | 0.341 |
MOD_NEK2_1 | 343 | 348 | PF00069 | 0.478 |
MOD_NEK2_1 | 39 | 44 | PF00069 | 0.513 |
MOD_NEK2_1 | 430 | 435 | PF00069 | 0.551 |
MOD_NEK2_1 | 441 | 446 | PF00069 | 0.534 |
MOD_NEK2_1 | 451 | 456 | PF00069 | 0.403 |
MOD_NEK2_1 | 464 | 469 | PF00069 | 0.299 |
MOD_NEK2_1 | 515 | 520 | PF00069 | 0.591 |
MOD_PIKK_1 | 296 | 302 | PF00454 | 0.514 |
MOD_PIKK_1 | 371 | 377 | PF00454 | 0.560 |
MOD_PIKK_1 | 441 | 447 | PF00454 | 0.558 |
MOD_PIKK_1 | 508 | 514 | PF00454 | 0.526 |
MOD_PKA_1 | 371 | 377 | PF00069 | 0.560 |
MOD_PKA_2 | 189 | 195 | PF00069 | 0.346 |
MOD_PKA_2 | 296 | 302 | PF00069 | 0.514 |
MOD_PKA_2 | 403 | 409 | PF00069 | 0.630 |
MOD_PKA_2 | 68 | 74 | PF00069 | 0.474 |
MOD_Plk_1 | 95 | 101 | PF00069 | 0.489 |
MOD_Plk_2-3 | 218 | 224 | PF00069 | 0.444 |
MOD_Plk_4 | 110 | 116 | PF00069 | 0.435 |
MOD_Plk_4 | 154 | 160 | PF00069 | 0.619 |
MOD_Plk_4 | 202 | 208 | PF00069 | 0.403 |
MOD_Plk_4 | 241 | 247 | PF00069 | 0.504 |
MOD_Plk_4 | 248 | 254 | PF00069 | 0.451 |
MOD_Plk_4 | 281 | 287 | PF00069 | 0.519 |
MOD_Plk_4 | 406 | 412 | PF00069 | 0.534 |
MOD_Plk_4 | 435 | 441 | PF00069 | 0.608 |
MOD_ProDKin_1 | 104 | 110 | PF00069 | 0.466 |
MOD_ProDKin_1 | 397 | 403 | PF00069 | 0.696 |
MOD_SUMO_for_1 | 364 | 367 | PF00179 | 0.705 |
MOD_SUMO_rev_2 | 367 | 374 | PF00179 | 0.548 |
TRG_DiLeu_BaLyEn_6 | 113 | 118 | PF01217 | 0.543 |
TRG_DiLeu_BaLyEn_6 | 277 | 282 | PF01217 | 0.592 |
TRG_DiLeu_BaLyEn_6 | 469 | 474 | PF01217 | 0.264 |
TRG_ENDOCYTIC_2 | 132 | 135 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 19 | 22 | PF00928 | 0.379 |
TRG_ENDOCYTIC_2 | 195 | 198 | PF00928 | 0.365 |
TRG_ENDOCYTIC_2 | 228 | 231 | PF00928 | 0.507 |
TRG_ENDOCYTIC_2 | 31 | 34 | PF00928 | 0.565 |
TRG_ENDOCYTIC_2 | 313 | 316 | PF00928 | 0.494 |
TRG_ENDOCYTIC_2 | 326 | 329 | PF00928 | 0.310 |
TRG_ENDOCYTIC_2 | 344 | 347 | PF00928 | 0.460 |
TRG_ENDOCYTIC_2 | 36 | 39 | PF00928 | 0.451 |
TRG_ENDOCYTIC_2 | 408 | 411 | PF00928 | 0.589 |
TRG_ENDOCYTIC_2 | 457 | 460 | PF00928 | 0.411 |
TRG_ER_diArg_1 | 320 | 322 | PF00400 | 0.466 |
TRG_ER_diArg_1 | 350 | 352 | PF00400 | 0.689 |
TRG_ER_diArg_1 | 355 | 358 | PF00400 | 0.643 |
TRG_ER_diLys_1 | 529 | 532 | PF00400 | 0.590 |
TRG_NLS_MonoExtN_4 | 357 | 364 | PF00514 | 0.574 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7X8X9 | Leishmania donovani | 82% | 100% |
A0A422NIA4 | Trypanosoma rangeli | 37% | 97% |
A4IAY2 | Leishmania infantum | 82% | 100% |
E9AER0 | Leishmania major | 83% | 100% |
E9B5W5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |