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:0016020 | membrane | 2 | 5 |
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 |
Related structures:
AlphaFold database: Q4Q3U9
Term | Name | Level | Count |
---|---|---|---|
GO:0006996 | organelle organization | 4 | 2 |
GO:0007030 | Golgi organization | 5 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 137 | 141 | PF00656 | 0.385 |
CLV_NRD_NRD_1 | 207 | 209 | PF00675 | 0.385 |
CLV_PCSK_KEX2_1 | 537 | 539 | PF00082 | 0.671 |
CLV_PCSK_PC1ET2_1 | 537 | 539 | PF00082 | 0.649 |
CLV_PCSK_SKI1_1 | 203 | 207 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 209 | 213 | PF00082 | 0.365 |
CLV_PCSK_SKI1_1 | 75 | 79 | PF00082 | 0.434 |
CLV_PCSK_SKI1_1 | 83 | 87 | PF00082 | 0.402 |
DEG_SPOP_SBC_1 | 462 | 466 | PF00917 | 0.568 |
DOC_CKS1_1 | 289 | 294 | PF01111 | 0.509 |
DOC_CYCLIN_yCln2_LP_2 | 525 | 531 | PF00134 | 0.664 |
DOC_MAPK_DCC_7 | 216 | 224 | PF00069 | 0.276 |
DOC_MAPK_MEF2A_6 | 216 | 224 | PF00069 | 0.276 |
DOC_MAPK_MEF2A_6 | 520 | 527 | PF00069 | 0.654 |
DOC_PP2B_LxvP_1 | 335 | 338 | PF13499 | 0.555 |
DOC_PP4_MxPP_1 | 521 | 524 | PF00568 | 0.646 |
DOC_USP7_MATH_1 | 158 | 162 | PF00917 | 0.342 |
DOC_USP7_MATH_1 | 277 | 281 | PF00917 | 0.427 |
DOC_USP7_MATH_1 | 331 | 335 | PF00917 | 0.678 |
DOC_USP7_MATH_1 | 363 | 367 | PF00917 | 0.708 |
DOC_USP7_MATH_1 | 462 | 466 | PF00917 | 0.652 |
DOC_USP7_MATH_1 | 469 | 473 | PF00917 | 0.644 |
DOC_USP7_MATH_1 | 494 | 498 | PF00917 | 0.637 |
DOC_WW_Pin1_4 | 153 | 158 | PF00397 | 0.492 |
DOC_WW_Pin1_4 | 288 | 293 | PF00397 | 0.500 |
DOC_WW_Pin1_4 | 306 | 311 | PF00397 | 0.620 |
DOC_WW_Pin1_4 | 347 | 352 | PF00397 | 0.791 |
DOC_WW_Pin1_4 | 426 | 431 | PF00397 | 0.698 |
DOC_WW_Pin1_4 | 471 | 476 | PF00397 | 0.744 |
DOC_WW_Pin1_4 | 53 | 58 | PF00397 | 0.442 |
LIG_APCC_ABBA_1 | 421 | 426 | PF00400 | 0.566 |
LIG_APCC_ABBA_1 | 63 | 68 | PF00400 | 0.406 |
LIG_BIR_III_2 | 140 | 144 | PF00653 | 0.385 |
LIG_BIR_III_4 | 404 | 408 | PF00653 | 0.583 |
LIG_CtBP_PxDLS_1 | 38 | 42 | PF00389 | 0.434 |
LIG_deltaCOP1_diTrp_1 | 196 | 204 | PF00928 | 0.385 |
LIG_EH_1 | 421 | 425 | PF12763 | 0.696 |
LIG_EH1_1 | 46 | 54 | PF00400 | 0.430 |
LIG_EVH1_2 | 523 | 527 | PF00568 | 0.652 |
LIG_FHA_1 | 103 | 109 | PF00498 | 0.385 |
LIG_FHA_1 | 254 | 260 | PF00498 | 0.385 |
LIG_FHA_1 | 265 | 271 | PF00498 | 0.416 |
LIG_FHA_1 | 307 | 313 | PF00498 | 0.786 |
LIG_FHA_2 | 110 | 116 | PF00498 | 0.342 |
LIG_FHA_2 | 135 | 141 | PF00498 | 0.527 |
LIG_FHA_2 | 174 | 180 | PF00498 | 0.356 |
LIG_FHA_2 | 232 | 238 | PF00498 | 0.385 |
LIG_FHA_2 | 242 | 248 | PF00498 | 0.274 |
LIG_FHA_2 | 69 | 75 | PF00498 | 0.464 |
LIG_GBD_Chelix_1 | 69 | 77 | PF00786 | 0.302 |
LIG_LIR_Apic_2 | 115 | 120 | PF02991 | 0.385 |
LIG_LIR_Apic_2 | 497 | 501 | PF02991 | 0.637 |
LIG_LIR_Gen_1 | 190 | 197 | PF02991 | 0.385 |
LIG_LIR_Gen_1 | 280 | 290 | PF02991 | 0.490 |
LIG_LIR_Gen_1 | 429 | 440 | PF02991 | 0.695 |
LIG_LIR_Gen_1 | 45 | 54 | PF02991 | 0.390 |
LIG_LIR_Nem_3 | 104 | 109 | PF02991 | 0.311 |
LIG_LIR_Nem_3 | 110 | 116 | PF02991 | 0.316 |
LIG_LIR_Nem_3 | 190 | 195 | PF02991 | 0.527 |
LIG_LIR_Nem_3 | 280 | 285 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 429 | 435 | PF02991 | 0.671 |
LIG_LIR_Nem_3 | 45 | 50 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 464 | 470 | PF02991 | 0.657 |
LIG_LIR_Nem_3 | 87 | 92 | PF02991 | 0.375 |
LIG_LYPXL_yS_3 | 467 | 470 | PF13949 | 0.631 |
LIG_PCNA_yPIPBox_3 | 178 | 189 | PF02747 | 0.385 |
LIG_REV1ctd_RIR_1 | 86 | 94 | PF16727 | 0.453 |
LIG_SH2_CRK | 117 | 121 | PF00017 | 0.385 |
LIG_SH2_CRK | 387 | 391 | PF00017 | 0.608 |
LIG_SH2_CRK | 498 | 502 | PF00017 | 0.564 |
LIG_SH2_NCK_1 | 387 | 391 | PF00017 | 0.608 |
LIG_SH2_NCK_1 | 498 | 502 | PF00017 | 0.565 |
LIG_SH2_SRC | 170 | 173 | PF00017 | 0.342 |
LIG_SH2_STAP1 | 109 | 113 | PF00017 | 0.342 |
LIG_SH2_STAP1 | 463 | 467 | PF00017 | 0.666 |
LIG_SH2_STAT5 | 117 | 120 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 170 | 173 | PF00017 | 0.385 |
LIG_SH2_STAT5 | 192 | 195 | PF00017 | 0.254 |
LIG_SH2_STAT5 | 92 | 95 | PF00017 | 0.378 |
LIG_SH3_1 | 498 | 504 | PF00018 | 0.621 |
LIG_SH3_1 | 51 | 57 | PF00018 | 0.444 |
LIG_SH3_3 | 214 | 220 | PF00018 | 0.385 |
LIG_SH3_3 | 286 | 292 | PF00018 | 0.557 |
LIG_SH3_3 | 330 | 336 | PF00018 | 0.691 |
LIG_SH3_3 | 345 | 351 | PF00018 | 0.676 |
LIG_SH3_3 | 356 | 362 | PF00018 | 0.623 |
LIG_SH3_3 | 367 | 373 | PF00018 | 0.586 |
LIG_SH3_3 | 394 | 400 | PF00018 | 0.663 |
LIG_SH3_3 | 417 | 423 | PF00018 | 0.654 |
LIG_SH3_3 | 498 | 504 | PF00018 | 0.806 |
LIG_SH3_3 | 51 | 57 | PF00018 | 0.444 |
LIG_SH3_3 | 525 | 531 | PF00018 | 0.664 |
LIG_SUMO_SIM_anti_2 | 179 | 187 | PF11976 | 0.342 |
LIG_SUMO_SIM_par_1 | 148 | 154 | PF11976 | 0.527 |
LIG_TRAF2_1 | 176 | 179 | PF00917 | 0.356 |
LIG_TRAF2_1 | 234 | 237 | PF00917 | 0.342 |
LIG_UBA3_1 | 181 | 189 | PF00899 | 0.385 |
LIG_WRC_WIRS_1 | 103 | 108 | PF05994 | 0.342 |
LIG_WRC_WIRS_1 | 392 | 397 | PF05994 | 0.647 |
LIG_WRC_WIRS_1 | 513 | 518 | PF05994 | 0.624 |
LIG_WW_3 | 371 | 375 | PF00397 | 0.639 |
LIG_WW_3 | 399 | 403 | PF00397 | 0.651 |
MOD_CDK_SPxK_1 | 288 | 294 | PF00069 | 0.506 |
MOD_CDK_SPxxK_3 | 53 | 60 | PF00069 | 0.447 |
MOD_CK1_1 | 253 | 259 | PF00069 | 0.385 |
MOD_CK1_1 | 26 | 32 | PF00069 | 0.652 |
MOD_CK1_1 | 264 | 270 | PF00069 | 0.398 |
MOD_CK1_1 | 288 | 294 | PF00069 | 0.506 |
MOD_CK1_1 | 322 | 328 | PF00069 | 0.672 |
MOD_CK1_1 | 388 | 394 | PF00069 | 0.572 |
MOD_CK1_1 | 471 | 477 | PF00069 | 0.602 |
MOD_CK2_1 | 173 | 179 | PF00069 | 0.356 |
MOD_CK2_1 | 231 | 237 | PF00069 | 0.513 |
MOD_CK2_1 | 241 | 247 | PF00069 | 0.316 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.601 |
MOD_GlcNHglycan | 30 | 33 | PF01048 | 0.600 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.593 |
MOD_GlcNHglycan | 477 | 480 | PF01048 | 0.714 |
MOD_GlcNHglycan | 498 | 501 | PF01048 | 0.637 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.487 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.406 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.385 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.527 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.666 |
MOD_GSK3_1 | 471 | 478 | PF00069 | 0.576 |
MOD_GSK3_1 | 490 | 497 | PF00069 | 0.614 |
MOD_GSK3_1 | 508 | 515 | PF00069 | 0.716 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.456 |
MOD_N-GLC_1 | 485 | 490 | PF02516 | 0.699 |
MOD_N-GLC_2 | 365 | 367 | PF02516 | 0.590 |
MOD_NEK2_1 | 184 | 189 | PF00069 | 0.342 |
MOD_NEK2_1 | 477 | 482 | PF00069 | 0.617 |
MOD_NEK2_1 | 485 | 490 | PF00069 | 0.634 |
MOD_NEK2_1 | 508 | 513 | PF00069 | 0.663 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.454 |
MOD_NEK2_2 | 84 | 89 | PF00069 | 0.407 |
MOD_NMyristoyl | 1 | 7 | PF02799 | 0.663 |
MOD_PIKK_1 | 184 | 190 | PF00454 | 0.342 |
MOD_PIKK_1 | 319 | 325 | PF00454 | 0.660 |
MOD_PIKK_1 | 469 | 475 | PF00454 | 0.636 |
MOD_PIKK_1 | 515 | 521 | PF00454 | 0.802 |
MOD_PK_1 | 281 | 287 | PF00069 | 0.544 |
MOD_Plk_1 | 21 | 27 | PF00069 | 0.675 |
MOD_Plk_1 | 304 | 310 | PF00069 | 0.643 |
MOD_Plk_2-3 | 231 | 237 | PF00069 | 0.385 |
MOD_Plk_4 | 177 | 183 | PF00069 | 0.342 |
MOD_Plk_4 | 285 | 291 | PF00069 | 0.597 |
MOD_Plk_4 | 84 | 90 | PF00069 | 0.448 |
MOD_ProDKin_1 | 153 | 159 | PF00069 | 0.492 |
MOD_ProDKin_1 | 288 | 294 | PF00069 | 0.506 |
MOD_ProDKin_1 | 306 | 312 | PF00069 | 0.623 |
MOD_ProDKin_1 | 347 | 353 | PF00069 | 0.791 |
MOD_ProDKin_1 | 426 | 432 | PF00069 | 0.697 |
MOD_ProDKin_1 | 471 | 477 | PF00069 | 0.747 |
MOD_ProDKin_1 | 53 | 59 | PF00069 | 0.442 |
MOD_SUMO_rev_2 | 201 | 211 | PF00179 | 0.342 |
MOD_SUMO_rev_2 | 79 | 85 | PF00179 | 0.424 |
TRG_DiLeu_BaLyEn_6 | 48 | 53 | PF01217 | 0.428 |
TRG_ENDOCYTIC_2 | 113 | 116 | PF00928 | 0.385 |
TRG_ENDOCYTIC_2 | 192 | 195 | PF00928 | 0.527 |
TRG_ENDOCYTIC_2 | 432 | 435 | PF00928 | 0.673 |
TRG_ENDOCYTIC_2 | 467 | 470 | PF00928 | 0.653 |
TRG_NES_CRM1_1 | 68 | 81 | PF08389 | 0.425 |
TRG_Pf-PMV_PEXEL_1 | 51 | 55 | PF00026 | 0.439 |
TRG_Pf-PMV_PEXEL_1 | 75 | 79 | PF00026 | 0.347 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IU65 | Leishmania donovani | 87% | 100% |
A4HLV0 | Leishmania braziliensis | 66% | 100% |
E9AHQ6 | Leishmania infantum | 88% | 100% |
E9B477 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 99% |