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: 5 |
NetGPI | no | yes: 0, no: 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005794 | Golgi apparatus | 5 | 6 |
GO:0043226 | organelle | 2 | 6 |
GO:0043227 | membrane-bounded organelle | 3 | 6 |
GO:0043229 | intracellular organelle | 3 | 6 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
GO:0016020 | membrane | 2 | 4 |
Related structures:
AlphaFold database: E9AHQ6
Term | Name | Level | Count |
---|---|---|---|
GO:0006996 | organelle organization | 4 | 1 |
GO:0007030 | Golgi organization | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 137 | 141 | PF00656 | 0.405 |
CLV_C14_Caspase3-7 | 244 | 248 | PF00656 | 0.296 |
CLV_NRD_NRD_1 | 207 | 209 | PF00675 | 0.405 |
CLV_NRD_NRD_1 | 280 | 282 | PF00675 | 0.365 |
CLV_NRD_NRD_1 | 287 | 289 | PF00675 | 0.495 |
CLV_PCSK_KEX2_1 | 287 | 289 | PF00082 | 0.520 |
CLV_PCSK_KEX2_1 | 538 | 540 | PF00082 | 0.682 |
CLV_PCSK_PC1ET2_1 | 538 | 540 | PF00082 | 0.658 |
CLV_PCSK_SKI1_1 | 203 | 207 | PF00082 | 0.405 |
CLV_PCSK_SKI1_1 | 209 | 213 | PF00082 | 0.343 |
CLV_PCSK_SKI1_1 | 75 | 79 | PF00082 | 0.448 |
CLV_PCSK_SKI1_1 | 83 | 87 | PF00082 | 0.368 |
DOC_CYCLIN_yCln2_LP_2 | 309 | 315 | PF00134 | 0.589 |
DOC_CYCLIN_yCln2_LP_2 | 35 | 41 | PF00134 | 0.404 |
DOC_CYCLIN_yCln2_LP_2 | 526 | 532 | PF00134 | 0.683 |
DOC_CYCLIN_yCln2_LP_2 | 97 | 103 | PF00134 | 0.323 |
DOC_MAPK_FxFP_2 | 466 | 469 | PF00069 | 0.556 |
DOC_MAPK_MEF2A_6 | 521 | 528 | PF00069 | 0.673 |
DOC_PP2B_LxvP_1 | 35 | 38 | PF13499 | 0.439 |
DOC_PP4_FxxP_1 | 466 | 469 | PF00568 | 0.556 |
DOC_PP4_MxPP_1 | 522 | 525 | PF00568 | 0.665 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.585 |
DOC_USP7_MATH_1 | 158 | 162 | PF00917 | 0.356 |
DOC_USP7_MATH_1 | 21 | 25 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 273 | 277 | PF00917 | 0.548 |
DOC_USP7_MATH_1 | 364 | 368 | PF00917 | 0.722 |
DOC_USP7_MATH_1 | 392 | 396 | PF00917 | 0.628 |
DOC_USP7_MATH_1 | 470 | 474 | PF00917 | 0.621 |
DOC_USP7_MATH_1 | 497 | 501 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 516 | 520 | PF00917 | 0.564 |
DOC_WW_Pin1_4 | 153 | 158 | PF00397 | 0.405 |
DOC_WW_Pin1_4 | 335 | 340 | PF00397 | 0.632 |
DOC_WW_Pin1_4 | 348 | 353 | PF00397 | 0.663 |
DOC_WW_Pin1_4 | 427 | 432 | PF00397 | 0.702 |
DOC_WW_Pin1_4 | 501 | 506 | PF00397 | 0.575 |
DOC_WW_Pin1_4 | 53 | 58 | PF00397 | 0.546 |
LIG_14-3-3_CanoR_1 | 23 | 30 | PF00244 | 0.525 |
LIG_14-3-3_CanoR_1 | 281 | 287 | PF00244 | 0.414 |
LIG_APCC_ABBA_1 | 63 | 68 | PF00400 | 0.421 |
LIG_BIR_III_2 | 140 | 144 | PF00653 | 0.405 |
LIG_BRCT_BRCA1_1 | 462 | 466 | PF00533 | 0.573 |
LIG_CtBP_PxDLS_1 | 38 | 42 | PF00389 | 0.431 |
LIG_deltaCOP1_diTrp_1 | 196 | 204 | PF00928 | 0.525 |
LIG_EH_1 | 422 | 426 | PF12763 | 0.704 |
LIG_EH1_1 | 46 | 54 | PF00400 | 0.438 |
LIG_EVH1_2 | 524 | 528 | PF00568 | 0.677 |
LIG_FHA_1 | 103 | 109 | PF00498 | 0.501 |
LIG_FHA_1 | 254 | 260 | PF00498 | 0.405 |
LIG_FHA_1 | 308 | 314 | PF00498 | 0.693 |
LIG_FHA_2 | 110 | 116 | PF00498 | 0.356 |
LIG_FHA_2 | 135 | 141 | PF00498 | 0.405 |
LIG_FHA_2 | 174 | 180 | PF00498 | 0.356 |
LIG_FHA_2 | 232 | 238 | PF00498 | 0.407 |
LIG_FHA_2 | 242 | 248 | PF00498 | 0.311 |
LIG_FHA_2 | 265 | 271 | PF00498 | 0.420 |
LIG_FHA_2 | 69 | 75 | PF00498 | 0.439 |
LIG_LIR_Apic_2 | 115 | 120 | PF02991 | 0.405 |
LIG_LIR_Apic_2 | 367 | 371 | PF02991 | 0.658 |
LIG_LIR_Apic_2 | 463 | 469 | PF02991 | 0.564 |
LIG_LIR_Gen_1 | 190 | 197 | PF02991 | 0.405 |
LIG_LIR_Gen_1 | 430 | 441 | PF02991 | 0.689 |
LIG_LIR_Gen_1 | 45 | 55 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 104 | 109 | PF02991 | 0.390 |
LIG_LIR_Nem_3 | 110 | 116 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 190 | 195 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 430 | 436 | PF02991 | 0.649 |
LIG_LIR_Nem_3 | 45 | 50 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 465 | 471 | PF02991 | 0.643 |
LIG_LYPXL_yS_3 | 468 | 471 | PF13949 | 0.610 |
LIG_PCNA_yPIPBox_3 | 178 | 189 | PF02747 | 0.405 |
LIG_REV1ctd_RIR_1 | 86 | 94 | PF16727 | 0.466 |
LIG_SH2_CRK | 117 | 121 | PF00017 | 0.405 |
LIG_SH2_CRK | 388 | 392 | PF00017 | 0.616 |
LIG_SH2_NCK_1 | 388 | 392 | PF00017 | 0.616 |
LIG_SH2_SRC | 170 | 173 | PF00017 | 0.356 |
LIG_SH2_STAP1 | 109 | 113 | PF00017 | 0.356 |
LIG_SH2_STAP1 | 464 | 468 | PF00017 | 0.654 |
LIG_SH2_STAT5 | 117 | 120 | PF00017 | 0.385 |
LIG_SH2_STAT5 | 170 | 173 | PF00017 | 0.405 |
LIG_SH3_1 | 368 | 374 | PF00018 | 0.608 |
LIG_SH3_1 | 51 | 57 | PF00018 | 0.455 |
LIG_SH3_3 | 214 | 220 | PF00018 | 0.405 |
LIG_SH3_3 | 287 | 293 | PF00018 | 0.704 |
LIG_SH3_3 | 331 | 337 | PF00018 | 0.716 |
LIG_SH3_3 | 346 | 352 | PF00018 | 0.548 |
LIG_SH3_3 | 357 | 363 | PF00018 | 0.624 |
LIG_SH3_3 | 368 | 374 | PF00018 | 0.585 |
LIG_SH3_3 | 395 | 401 | PF00018 | 0.665 |
LIG_SH3_3 | 418 | 424 | PF00018 | 0.659 |
LIG_SH3_3 | 499 | 505 | PF00018 | 0.702 |
LIG_SH3_3 | 51 | 57 | PF00018 | 0.560 |
LIG_SH3_3 | 526 | 532 | PF00018 | 0.683 |
LIG_SUMO_SIM_anti_2 | 179 | 187 | PF11976 | 0.356 |
LIG_SUMO_SIM_par_1 | 148 | 154 | PF11976 | 0.405 |
LIG_SxIP_EBH_1 | 507 | 521 | PF03271 | 0.568 |
LIG_TRAF2_1 | 176 | 179 | PF00917 | 0.356 |
LIG_TRAF2_1 | 234 | 237 | PF00917 | 0.356 |
LIG_TRAF2_1 | 338 | 341 | PF00917 | 0.608 |
LIG_UBA3_1 | 181 | 189 | PF00899 | 0.519 |
LIG_UBA3_1 | 69 | 75 | PF00899 | 0.330 |
LIG_WRC_WIRS_1 | 103 | 108 | PF05994 | 0.356 |
LIG_WRC_WIRS_1 | 393 | 398 | PF05994 | 0.651 |
LIG_WW_3 | 332 | 336 | PF00397 | 0.589 |
LIG_WW_3 | 372 | 376 | PF00397 | 0.643 |
LIG_WW_3 | 400 | 404 | PF00397 | 0.651 |
MOD_CDK_SPxxK_3 | 53 | 60 | PF00069 | 0.459 |
MOD_CK1_1 | 253 | 259 | PF00069 | 0.405 |
MOD_CK1_1 | 26 | 32 | PF00069 | 0.757 |
MOD_CK1_1 | 264 | 270 | PF00069 | 0.447 |
MOD_CK1_1 | 323 | 329 | PF00069 | 0.685 |
MOD_CK2_1 | 173 | 179 | PF00069 | 0.363 |
MOD_CK2_1 | 190 | 196 | PF00069 | 0.271 |
MOD_CK2_1 | 231 | 237 | PF00069 | 0.407 |
MOD_CK2_1 | 335 | 341 | PF00069 | 0.611 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.645 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.716 |
MOD_GlcNHglycan | 267 | 270 | PF01048 | 0.538 |
MOD_GlcNHglycan | 30 | 33 | PF01048 | 0.662 |
MOD_GlcNHglycan | 478 | 481 | PF01048 | 0.708 |
MOD_GlcNHglycan | 499 | 502 | PF01048 | 0.641 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.376 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.356 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.405 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.398 |
MOD_GSK3_1 | 282 | 289 | PF00069 | 0.550 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.670 |
MOD_GSK3_1 | 456 | 463 | PF00069 | 0.598 |
MOD_GSK3_1 | 497 | 504 | PF00069 | 0.637 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.422 |
MOD_N-GLC_1 | 231 | 236 | PF02516 | 0.320 |
MOD_N-GLC_1 | 486 | 491 | PF02516 | 0.690 |
MOD_NEK2_1 | 184 | 189 | PF00069 | 0.356 |
MOD_NEK2_1 | 486 | 491 | PF00069 | 0.617 |
MOD_NEK2_1 | 509 | 514 | PF00069 | 0.661 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.460 |
MOD_NEK2_2 | 84 | 89 | PF00069 | 0.418 |
MOD_NMyristoyl | 1 | 7 | PF02799 | 0.695 |
MOD_PIKK_1 | 184 | 190 | PF00454 | 0.356 |
MOD_PIKK_1 | 320 | 326 | PF00454 | 0.663 |
MOD_PIKK_1 | 327 | 333 | PF00454 | 0.633 |
MOD_PIKK_1 | 470 | 476 | PF00454 | 0.609 |
MOD_PIKK_1 | 516 | 522 | PF00454 | 0.691 |
MOD_PK_1 | 282 | 288 | PF00069 | 0.568 |
MOD_PKA_2 | 286 | 292 | PF00069 | 0.526 |
MOD_Plk_1 | 21 | 27 | PF00069 | 0.667 |
MOD_Plk_1 | 231 | 237 | PF00069 | 0.280 |
MOD_Plk_1 | 305 | 311 | PF00069 | 0.651 |
MOD_Plk_1 | 324 | 330 | PF00069 | 0.546 |
MOD_Plk_1 | 460 | 466 | PF00069 | 0.592 |
MOD_Plk_2-3 | 231 | 237 | PF00069 | 0.405 |
MOD_Plk_4 | 177 | 183 | PF00069 | 0.367 |
MOD_Plk_4 | 261 | 267 | PF00069 | 0.272 |
MOD_Plk_4 | 84 | 90 | PF00069 | 0.458 |
MOD_ProDKin_1 | 153 | 159 | PF00069 | 0.405 |
MOD_ProDKin_1 | 335 | 341 | PF00069 | 0.633 |
MOD_ProDKin_1 | 348 | 354 | PF00069 | 0.661 |
MOD_ProDKin_1 | 427 | 433 | PF00069 | 0.699 |
MOD_ProDKin_1 | 501 | 507 | PF00069 | 0.575 |
MOD_ProDKin_1 | 53 | 59 | PF00069 | 0.545 |
MOD_SUMO_rev_2 | 201 | 211 | PF00179 | 0.356 |
MOD_SUMO_rev_2 | 79 | 85 | PF00179 | 0.433 |
TRG_DiLeu_BaLyEn_6 | 48 | 53 | PF01217 | 0.436 |
TRG_ENDOCYTIC_2 | 113 | 116 | PF00928 | 0.405 |
TRG_ENDOCYTIC_2 | 192 | 195 | PF00928 | 0.405 |
TRG_ENDOCYTIC_2 | 433 | 436 | PF00928 | 0.641 |
TRG_ENDOCYTIC_2 | 468 | 471 | PF00928 | 0.634 |
TRG_ER_diArg_1 | 286 | 288 | PF00400 | 0.534 |
TRG_NES_CRM1_1 | 68 | 81 | PF08389 | 0.437 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IU65 | Leishmania donovani | 100% | 100% |
A4HLV0 | Leishmania braziliensis | 67% | 100% |
E9B477 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
Q4Q3U9 | Leishmania major | 88% | 100% |