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:0005789 | endoplasmic reticulum membrane | 4 | 6 |
GO:0016020 | membrane | 2 | 7 |
GO:0031090 | organelle membrane | 3 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
GO:0005785 | signal recognition particle receptor complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0098796 | membrane protein complex | 2 | 1 |
GO:0140534 | endoplasmic reticulum protein-containing complex | 2 | 1 |
Related structures:
AlphaFold database: A0A3S7X750
Term | Name | Level | Count |
---|---|---|---|
GO:0006605 | protein targeting | 5 | 1 |
GO:0006810 | transport | 3 | 1 |
GO:0006886 | intracellular protein transport | 4 | 1 |
GO:0008104 | protein localization | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0015031 | protein transport | 4 | 1 |
GO:0033036 | macromolecule localization | 2 | 1 |
GO:0033365 | protein localization to organelle | 5 | 1 |
GO:0045047 | protein targeting to ER | 6 | 1 |
GO:0045184 | establishment of protein localization | 3 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
GO:0070727 | cellular macromolecule localization | 3 | 1 |
GO:0070972 | protein localization to endoplasmic reticulum | 6 | 1 |
GO:0071702 | organic substance transport | 4 | 1 |
GO:0071705 | nitrogen compound transport | 4 | 1 |
GO:0072594 | establishment of protein localization to organelle | 4 | 1 |
GO:0072599 | establishment of protein localization to endoplasmic reticulum | 5 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 7 |
GO:0003676 | nucleic acid binding | 3 | 2 |
GO:0003746 | translation elongation factor activity | 4 | 2 |
GO:0005488 | binding | 1 | 7 |
GO:0005525 | GTP binding | 5 | 7 |
GO:0008135 | translation factor activity, RNA binding | 3 | 2 |
GO:0017076 | purine nucleotide binding | 4 | 7 |
GO:0019001 | guanyl nucleotide binding | 5 | 7 |
GO:0032553 | ribonucleotide binding | 3 | 7 |
GO:0032555 | purine ribonucleotide binding | 4 | 7 |
GO:0032561 | guanyl ribonucleotide binding | 5 | 7 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 7 |
GO:0036094 | small molecule binding | 2 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043168 | anion binding | 3 | 7 |
GO:0045182 | translation regulator activity | 1 | 2 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 2 |
GO:0097159 | organic cyclic compound binding | 2 | 7 |
GO:0097367 | carbohydrate derivative binding | 2 | 7 |
GO:1901265 | nucleoside phosphate binding | 3 | 7 |
GO:1901363 | heterocyclic compound binding | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 321 | 325 | PF00656 | 0.469 |
CLV_C14_Caspase3-7 | 394 | 398 | PF00656 | 0.459 |
CLV_C14_Caspase3-7 | 425 | 429 | PF00656 | 0.629 |
CLV_NRD_NRD_1 | 133 | 135 | PF00675 | 0.773 |
CLV_NRD_NRD_1 | 230 | 232 | PF00675 | 0.411 |
CLV_NRD_NRD_1 | 350 | 352 | PF00675 | 0.316 |
CLV_NRD_NRD_1 | 370 | 372 | PF00675 | 0.271 |
CLV_NRD_NRD_1 | 384 | 386 | PF00675 | 0.357 |
CLV_NRD_NRD_1 | 418 | 420 | PF00675 | 0.521 |
CLV_PCSK_KEX2_1 | 229 | 231 | PF00082 | 0.416 |
CLV_PCSK_KEX2_1 | 350 | 352 | PF00082 | 0.300 |
CLV_PCSK_KEX2_1 | 358 | 360 | PF00082 | 0.243 |
CLV_PCSK_KEX2_1 | 418 | 420 | PF00082 | 0.463 |
CLV_PCSK_PC1ET2_1 | 358 | 360 | PF00082 | 0.269 |
CLV_PCSK_SKI1_1 | 108 | 112 | PF00082 | 0.649 |
CLV_PCSK_SKI1_1 | 18 | 22 | PF00082 | 0.624 |
CLV_PCSK_SKI1_1 | 246 | 250 | PF00082 | 0.413 |
CLV_PCSK_SKI1_1 | 350 | 354 | PF00082 | 0.274 |
CLV_PCSK_SKI1_1 | 371 | 375 | PF00082 | 0.275 |
CLV_PCSK_SKI1_1 | 419 | 423 | PF00082 | 0.457 |
CLV_PCSK_SKI1_1 | 86 | 90 | PF00082 | 0.685 |
DEG_SPOP_SBC_1 | 232 | 236 | PF00917 | 0.516 |
DOC_CKS1_1 | 93 | 98 | PF01111 | 0.472 |
DOC_CYCLIN_RxL_1 | 348 | 357 | PF00134 | 0.469 |
DOC_CYCLIN_RxL_1 | 368 | 375 | PF00134 | 0.383 |
DOC_CYCLIN_yCln2_LP_2 | 459 | 465 | PF00134 | 0.538 |
DOC_MAPK_gen_1 | 134 | 141 | PF00069 | 0.399 |
DOC_MAPK_gen_1 | 229 | 239 | PF00069 | 0.469 |
DOC_MAPK_gen_1 | 418 | 424 | PF00069 | 0.657 |
DOC_MAPK_MEF2A_6 | 233 | 241 | PF00069 | 0.476 |
DOC_MAPK_MEF2A_6 | 246 | 253 | PF00069 | 0.528 |
DOC_PP1_RVXF_1 | 217 | 224 | PF00149 | 0.531 |
DOC_PP1_RVXF_1 | 348 | 355 | PF00149 | 0.472 |
DOC_PP2B_LxvP_1 | 459 | 462 | PF13499 | 0.545 |
DOC_USP7_MATH_1 | 120 | 124 | PF00917 | 0.427 |
DOC_USP7_MATH_1 | 183 | 187 | PF00917 | 0.410 |
DOC_USP7_MATH_1 | 447 | 451 | PF00917 | 0.684 |
DOC_USP7_MATH_1 | 63 | 67 | PF00917 | 0.440 |
DOC_USP7_MATH_1 | 98 | 102 | PF00917 | 0.466 |
DOC_USP7_UBL2_3 | 368 | 372 | PF12436 | 0.455 |
DOC_WW_Pin1_4 | 148 | 153 | PF00397 | 0.468 |
DOC_WW_Pin1_4 | 177 | 182 | PF00397 | 0.449 |
DOC_WW_Pin1_4 | 340 | 345 | PF00397 | 0.490 |
DOC_WW_Pin1_4 | 89 | 94 | PF00397 | 0.520 |
LIG_14-3-3_CanoR_1 | 108 | 117 | PF00244 | 0.413 |
LIG_14-3-3_CanoR_1 | 190 | 195 | PF00244 | 0.410 |
LIG_14-3-3_CanoR_1 | 230 | 239 | PF00244 | 0.480 |
LIG_14-3-3_CanoR_1 | 263 | 267 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 281 | 291 | PF00244 | 0.396 |
LIG_14-3-3_CanoR_1 | 419 | 425 | PF00244 | 0.595 |
LIG_14-3-3_CanoR_1 | 69 | 74 | PF00244 | 0.442 |
LIG_14-3-3_CanoR_1 | 86 | 93 | PF00244 | 0.488 |
LIG_14-3-3_CanoR_1 | 97 | 106 | PF00244 | 0.413 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.442 |
LIG_BIR_III_2 | 172 | 176 | PF00653 | 0.441 |
LIG_BRCT_BRCA1_1 | 342 | 346 | PF00533 | 0.469 |
LIG_BRCT_BRCA1_1 | 452 | 456 | PF00533 | 0.586 |
LIG_deltaCOP1_diTrp_1 | 198 | 201 | PF00928 | 0.316 |
LIG_EH1_1 | 346 | 354 | PF00400 | 0.469 |
LIG_eIF4E_1 | 347 | 353 | PF01652 | 0.469 |
LIG_FHA_1 | 149 | 155 | PF00498 | 0.436 |
LIG_FHA_1 | 203 | 209 | PF00498 | 0.369 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.472 |
LIG_FHA_1 | 283 | 289 | PF00498 | 0.534 |
LIG_FHA_2 | 10 | 16 | PF00498 | 0.417 |
LIG_FHA_2 | 319 | 325 | PF00498 | 0.555 |
LIG_FHA_2 | 355 | 361 | PF00498 | 0.474 |
LIG_GBD_Chelix_1 | 333 | 341 | PF00786 | 0.269 |
LIG_HCF-1_HBM_1 | 476 | 479 | PF13415 | 0.578 |
LIG_LIR_Gen_1 | 122 | 132 | PF02991 | 0.427 |
LIG_LIR_Gen_1 | 196 | 207 | PF02991 | 0.279 |
LIG_LIR_Gen_1 | 247 | 254 | PF02991 | 0.516 |
LIG_LIR_Gen_1 | 335 | 346 | PF02991 | 0.469 |
LIG_LIR_Gen_1 | 453 | 464 | PF02991 | 0.547 |
LIG_LIR_Nem_3 | 122 | 128 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 196 | 202 | PF02991 | 0.310 |
LIG_LIR_Nem_3 | 247 | 253 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 335 | 341 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 343 | 349 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 453 | 459 | PF02991 | 0.544 |
LIG_MAD2 | 289 | 297 | PF02301 | 0.516 |
LIG_SH2_SRC | 210 | 213 | PF00017 | 0.292 |
LIG_SH2_STAP1 | 365 | 369 | PF00017 | 0.455 |
LIG_SH2_STAP1 | 479 | 483 | PF00017 | 0.598 |
LIG_SH2_STAT5 | 210 | 213 | PF00017 | 0.304 |
LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.571 |
LIG_SH3_3 | 288 | 294 | PF00018 | 0.469 |
LIG_SH3_3 | 90 | 96 | PF00018 | 0.468 |
LIG_SUMO_SIM_anti_2 | 480 | 486 | PF11976 | 0.589 |
LIG_SUMO_SIM_par_1 | 312 | 319 | PF11976 | 0.469 |
LIG_SUMO_SIM_par_1 | 420 | 425 | PF11976 | 0.584 |
LIG_TRAF2_1 | 41 | 44 | PF00917 | 0.444 |
LIG_TYR_ITIM | 208 | 213 | PF00017 | 0.321 |
LIG_UBA3_1 | 238 | 246 | PF00899 | 0.479 |
LIG_WRC_WIRS_1 | 191 | 196 | PF05994 | 0.443 |
LIG_WW_3 | 436 | 440 | PF00397 | 0.692 |
MOD_CDK_SPK_2 | 92 | 97 | PF00069 | 0.439 |
MOD_CK1_1 | 192 | 198 | PF00069 | 0.446 |
MOD_CK1_1 | 244 | 250 | PF00069 | 0.481 |
MOD_CK1_1 | 262 | 268 | PF00069 | 0.469 |
MOD_CK1_1 | 282 | 288 | PF00069 | 0.387 |
MOD_CK1_1 | 32 | 38 | PF00069 | 0.548 |
MOD_CK1_1 | 364 | 370 | PF00069 | 0.462 |
MOD_CK1_1 | 381 | 387 | PF00069 | 0.469 |
MOD_CK1_1 | 450 | 456 | PF00069 | 0.596 |
MOD_CK2_1 | 192 | 198 | PF00069 | 0.432 |
MOD_CK2_1 | 262 | 268 | PF00069 | 0.455 |
MOD_CK2_1 | 38 | 44 | PF00069 | 0.497 |
MOD_CK2_1 | 9 | 15 | PF00069 | 0.416 |
MOD_Cter_Amidation | 416 | 419 | PF01082 | 0.479 |
MOD_GlcNHglycan | 100 | 103 | PF01048 | 0.661 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.660 |
MOD_GlcNHglycan | 195 | 198 | PF01048 | 0.576 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.314 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.287 |
MOD_GlcNHglycan | 268 | 272 | PF01048 | 0.310 |
MOD_GlcNHglycan | 31 | 34 | PF01048 | 0.763 |
MOD_GlcNHglycan | 413 | 416 | PF01048 | 0.505 |
MOD_GlcNHglycan | 449 | 452 | PF01048 | 0.431 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.669 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.534 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.424 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.451 |
MOD_LATS_1 | 279 | 285 | PF00433 | 0.469 |
MOD_LATS_1 | 84 | 90 | PF00433 | 0.487 |
MOD_N-GLC_1 | 108 | 113 | PF02516 | 0.636 |
MOD_N-GLC_1 | 282 | 287 | PF02516 | 0.269 |
MOD_N-GLC_1 | 9 | 14 | PF02516 | 0.651 |
MOD_NEK2_1 | 202 | 207 | PF00069 | 0.383 |
MOD_NEK2_1 | 259 | 264 | PF00069 | 0.469 |
MOD_NEK2_1 | 354 | 359 | PF00069 | 0.476 |
MOD_NEK2_1 | 47 | 52 | PF00069 | 0.425 |
MOD_PK_1 | 391 | 397 | PF00069 | 0.459 |
MOD_PKA_2 | 189 | 195 | PF00069 | 0.401 |
MOD_PKA_2 | 232 | 238 | PF00069 | 0.476 |
MOD_PKA_2 | 262 | 268 | PF00069 | 0.479 |
MOD_PKB_1 | 229 | 237 | PF00069 | 0.577 |
MOD_Plk_1 | 108 | 114 | PF00069 | 0.421 |
MOD_Plk_1 | 9 | 15 | PF00069 | 0.450 |
MOD_Plk_2-3 | 318 | 324 | PF00069 | 0.469 |
MOD_Plk_4 | 120 | 126 | PF00069 | 0.421 |
MOD_Plk_4 | 202 | 208 | PF00069 | 0.338 |
MOD_Plk_4 | 233 | 239 | PF00069 | 0.469 |
MOD_Plk_4 | 9 | 15 | PF00069 | 0.412 |
MOD_ProDKin_1 | 148 | 154 | PF00069 | 0.470 |
MOD_ProDKin_1 | 177 | 183 | PF00069 | 0.446 |
MOD_ProDKin_1 | 340 | 346 | PF00069 | 0.490 |
MOD_ProDKin_1 | 89 | 95 | PF00069 | 0.515 |
MOD_SUMO_rev_2 | 470 | 480 | PF00179 | 0.624 |
TRG_DiLeu_BaEn_1 | 43 | 48 | PF01217 | 0.435 |
TRG_DiLeu_BaLyEn_6 | 348 | 353 | PF01217 | 0.469 |
TRG_ENDOCYTIC_2 | 210 | 213 | PF00928 | 0.321 |
TRG_ER_diArg_1 | 229 | 231 | PF00400 | 0.616 |
TRG_ER_diArg_1 | 349 | 351 | PF00400 | 0.516 |
TRG_ER_diArg_1 | 418 | 420 | PF00400 | 0.647 |
TRG_Pf-PMV_PEXEL_1 | 305 | 309 | PF00026 | 0.284 |
TRG_Pf-PMV_PEXEL_1 | 371 | 375 | PF00026 | 0.269 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2X6 | Leptomonas seymouri | 53% | 100% |
A4HLX3 | Leishmania braziliensis | 69% | 100% |
A4I9A2 | Leishmania infantum | 100% | 100% |
E9B4A2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
Q4Q3S4 | Leishmania major | 92% | 100% |