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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0031974 | membrane-enclosed lumen | 2 | 2 |
GO:0031981 | nuclear lumen | 5 | 2 |
GO:0043233 | organelle lumen | 3 | 2 |
GO:0070013 | intracellular organelle lumen | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: E9ADN2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 162 | 166 | PF00656 | 0.655 |
CLV_C14_Caspase3-7 | 415 | 419 | PF00656 | 0.319 |
CLV_NRD_NRD_1 | 115 | 117 | PF00675 | 0.502 |
CLV_NRD_NRD_1 | 156 | 158 | PF00675 | 0.520 |
CLV_NRD_NRD_1 | 199 | 201 | PF00675 | 0.432 |
CLV_NRD_NRD_1 | 273 | 275 | PF00675 | 0.475 |
CLV_NRD_NRD_1 | 428 | 430 | PF00675 | 0.402 |
CLV_PCSK_KEX2_1 | 115 | 117 | PF00082 | 0.502 |
CLV_PCSK_KEX2_1 | 156 | 158 | PF00082 | 0.520 |
CLV_PCSK_KEX2_1 | 199 | 201 | PF00082 | 0.479 |
CLV_PCSK_KEX2_1 | 208 | 210 | PF00082 | 0.620 |
CLV_PCSK_PC1ET2_1 | 208 | 210 | PF00082 | 0.626 |
CLV_PCSK_SKI1_1 | 125 | 129 | PF00082 | 0.544 |
CLV_PCSK_SKI1_1 | 136 | 140 | PF00082 | 0.510 |
CLV_PCSK_SKI1_1 | 186 | 190 | PF00082 | 0.408 |
CLV_PCSK_SKI1_1 | 316 | 320 | PF00082 | 0.387 |
CLV_PCSK_SKI1_1 | 357 | 361 | PF00082 | 0.304 |
DEG_SPOP_SBC_1 | 169 | 173 | PF00917 | 0.549 |
DOC_CYCLIN_RxL_1 | 122 | 132 | PF00134 | 0.558 |
DOC_CYCLIN_yCln2_LP_2 | 44 | 50 | PF00134 | 0.443 |
DOC_MAPK_gen_1 | 115 | 121 | PF00069 | 0.484 |
DOC_MAPK_HePTP_8 | 112 | 128 | PF00069 | 0.476 |
DOC_PP1_RVXF_1 | 134 | 141 | PF00149 | 0.550 |
DOC_PP2B_LxvP_1 | 126 | 129 | PF13499 | 0.602 |
DOC_PP2B_LxvP_1 | 145 | 148 | PF13499 | 0.367 |
DOC_PP4_FxxP_1 | 260 | 263 | PF00568 | 0.445 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.714 |
DOC_USP7_MATH_1 | 204 | 208 | PF00917 | 0.480 |
DOC_USP7_MATH_1 | 251 | 255 | PF00917 | 0.654 |
DOC_USP7_MATH_1 | 304 | 308 | PF00917 | 0.325 |
DOC_USP7_MATH_1 | 359 | 363 | PF00917 | 0.408 |
DOC_USP7_MATH_1 | 374 | 378 | PF00917 | 0.272 |
DOC_USP7_MATH_1 | 93 | 97 | PF00917 | 0.708 |
DOC_USP7_MATH_2 | 300 | 306 | PF00917 | 0.363 |
DOC_USP7_UBL2_3 | 271 | 275 | PF12436 | 0.473 |
DOC_WW_Pin1_4 | 334 | 339 | PF00397 | 0.365 |
LIG_14-3-3_CanoR_1 | 209 | 216 | PF00244 | 0.664 |
LIG_14-3-3_CanoR_1 | 28 | 37 | PF00244 | 0.493 |
LIG_BIR_III_4 | 160 | 164 | PF00653 | 0.461 |
LIG_BIR_III_4 | 51 | 55 | PF00653 | 0.447 |
LIG_BRCT_BRCA1_1 | 256 | 260 | PF00533 | 0.481 |
LIG_deltaCOP1_diTrp_1 | 7 | 11 | PF00928 | 0.495 |
LIG_eIF4E_1 | 106 | 112 | PF01652 | 0.626 |
LIG_FHA_1 | 107 | 113 | PF00498 | 0.538 |
LIG_FHA_1 | 209 | 215 | PF00498 | 0.615 |
LIG_FHA_1 | 227 | 233 | PF00498 | 0.441 |
LIG_FHA_1 | 257 | 263 | PF00498 | 0.470 |
LIG_FHA_1 | 328 | 334 | PF00498 | 0.319 |
LIG_FHA_1 | 385 | 391 | PF00498 | 0.389 |
LIG_FHA_1 | 412 | 418 | PF00498 | 0.325 |
LIG_FHA_2 | 187 | 193 | PF00498 | 0.420 |
LIG_FHA_2 | 413 | 419 | PF00498 | 0.291 |
LIG_LIR_Apic_2 | 257 | 263 | PF02991 | 0.477 |
LIG_LIR_Gen_1 | 183 | 191 | PF02991 | 0.448 |
LIG_LIR_Gen_1 | 278 | 287 | PF02991 | 0.392 |
LIG_LIR_Gen_1 | 365 | 375 | PF02991 | 0.385 |
LIG_LIR_Gen_1 | 428 | 437 | PF02991 | 0.349 |
LIG_LIR_Nem_3 | 183 | 187 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 225 | 231 | PF02991 | 0.524 |
LIG_LIR_Nem_3 | 278 | 282 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 283 | 287 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 365 | 371 | PF02991 | 0.385 |
LIG_LYPXL_yS_3 | 141 | 144 | PF13949 | 0.507 |
LIG_MLH1_MIPbox_1 | 257 | 261 | PF16413 | 0.468 |
LIG_SH2_CRK | 228 | 232 | PF00017 | 0.452 |
LIG_SH2_CRK | 265 | 269 | PF00017 | 0.417 |
LIG_SH2_CRK | 279 | 283 | PF00017 | 0.447 |
LIG_SH2_GRB2like | 279 | 282 | PF00017 | 0.454 |
LIG_SH2_NCK_1 | 279 | 283 | PF00017 | 0.444 |
LIG_SH2_SRC | 279 | 282 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 184 | 187 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 228 | 231 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 328 | 331 | PF00017 | 0.367 |
LIG_SH2_STAT5 | 431 | 434 | PF00017 | 0.330 |
LIG_SH3_3 | 118 | 124 | PF00018 | 0.637 |
LIG_SH3_3 | 17 | 23 | PF00018 | 0.495 |
LIG_SH3_3 | 213 | 219 | PF00018 | 0.483 |
LIG_SH3_3 | 335 | 341 | PF00018 | 0.336 |
LIG_SH3_3 | 58 | 64 | PF00018 | 0.434 |
LIG_SH3_3 | 71 | 77 | PF00018 | 0.433 |
LIG_SUMO_SIM_par_1 | 391 | 398 | PF11976 | 0.291 |
LIG_TRAF2_2 | 148 | 153 | PF00917 | 0.470 |
LIG_TYR_ITIM | 182 | 187 | PF00017 | 0.437 |
LIG_UBA3_1 | 267 | 275 | PF00899 | 0.457 |
LIG_WRC_WIRS_1 | 360 | 365 | PF05994 | 0.222 |
LIG_WRC_WIRS_1 | 65 | 70 | PF05994 | 0.492 |
MOD_CK1_1 | 132 | 138 | PF00069 | 0.603 |
MOD_CK1_1 | 143 | 149 | PF00069 | 0.366 |
MOD_CK1_1 | 174 | 180 | PF00069 | 0.497 |
MOD_CK1_1 | 207 | 213 | PF00069 | 0.587 |
MOD_CK1_1 | 241 | 247 | PF00069 | 0.650 |
MOD_CK1_1 | 254 | 260 | PF00069 | 0.526 |
MOD_CK1_1 | 362 | 368 | PF00069 | 0.367 |
MOD_CK2_1 | 186 | 192 | PF00069 | 0.408 |
MOD_CMANNOS | 198 | 201 | PF00535 | 0.435 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.571 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.436 |
MOD_GlcNHglycan | 240 | 243 | PF01048 | 0.522 |
MOD_GlcNHglycan | 247 | 250 | PF01048 | 0.592 |
MOD_GlcNHglycan | 306 | 309 | PF01048 | 0.270 |
MOD_GlcNHglycan | 345 | 348 | PF01048 | 0.370 |
MOD_GlcNHglycan | 376 | 379 | PF01048 | 0.377 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.429 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.573 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.629 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.489 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.656 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.523 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.544 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.454 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.612 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.396 |
MOD_GSK3_1 | 394 | 401 | PF00069 | 0.291 |
MOD_GSK3_1 | 412 | 419 | PF00069 | 0.291 |
MOD_N-GLC_1 | 280 | 285 | PF02516 | 0.464 |
MOD_N-GLC_1 | 398 | 403 | PF02516 | 0.291 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.604 |
MOD_NEK2_1 | 353 | 358 | PF00069 | 0.367 |
MOD_NEK2_1 | 395 | 400 | PF00069 | 0.291 |
MOD_NEK2_1 | 411 | 416 | PF00069 | 0.291 |
MOD_NEK2_1 | 424 | 429 | PF00069 | 0.265 |
MOD_PKA_1 | 208 | 214 | PF00069 | 0.538 |
MOD_PKA_2 | 208 | 214 | PF00069 | 0.641 |
MOD_PKB_1 | 26 | 34 | PF00069 | 0.503 |
MOD_Plk_1 | 280 | 286 | PF00069 | 0.438 |
MOD_Plk_1 | 380 | 386 | PF00069 | 0.273 |
MOD_Plk_1 | 411 | 417 | PF00069 | 0.367 |
MOD_Plk_2-3 | 412 | 418 | PF00069 | 0.325 |
MOD_Plk_4 | 140 | 146 | PF00069 | 0.419 |
MOD_Plk_4 | 177 | 183 | PF00069 | 0.480 |
MOD_Plk_4 | 256 | 262 | PF00069 | 0.493 |
MOD_Plk_4 | 380 | 386 | PF00069 | 0.254 |
MOD_Plk_4 | 412 | 418 | PF00069 | 0.291 |
MOD_ProDKin_1 | 334 | 340 | PF00069 | 0.365 |
TRG_DiLeu_BaLyEn_6 | 122 | 127 | PF01217 | 0.739 |
TRG_DiLeu_BaLyEn_6 | 61 | 66 | PF01217 | 0.431 |
TRG_ENDOCYTIC_2 | 141 | 144 | PF00928 | 0.507 |
TRG_ENDOCYTIC_2 | 184 | 187 | PF00928 | 0.385 |
TRG_ENDOCYTIC_2 | 228 | 231 | PF00928 | 0.455 |
TRG_ENDOCYTIC_2 | 265 | 268 | PF00928 | 0.421 |
TRG_ENDOCYTIC_2 | 279 | 282 | PF00928 | 0.454 |
TRG_ENDOCYTIC_2 | 431 | 434 | PF00928 | 0.330 |
TRG_ER_diArg_1 | 123 | 126 | PF00400 | 0.605 |
TRG_ER_diArg_1 | 155 | 157 | PF00400 | 0.504 |
TRG_ER_diArg_1 | 198 | 200 | PF00400 | 0.473 |
TRG_ER_diArg_1 | 25 | 28 | PF00400 | 0.523 |
TRG_Pf-PMV_PEXEL_1 | 46 | 51 | PF00026 | 0.444 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I9L3 | Leptomonas seymouri | 57% | 100% |
A0A3S7X221 | Leishmania donovani | 93% | 100% |
A4HH57 | Leishmania braziliensis | 78% | 100% |
A4I483 | Leishmania infantum | 93% | 100% |
C9ZKP7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
E9AM48 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
V5BPX7 | Trypanosoma cruzi | 34% | 100% |