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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005840 | ribosome | 5 | 8 |
GO:0032991 | protein-containing complex | 1 | 8 |
GO:0043226 | organelle | 2 | 8 |
GO:0043228 | non-membrane-bounded organelle | 3 | 8 |
GO:0043229 | intracellular organelle | 3 | 8 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 8 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
GO:1990904 | ribonucleoprotein complex | 2 | 8 |
Related structures:
AlphaFold database: A4HCG2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 323 | 325 | PF00675 | 0.824 |
CLV_NRD_NRD_1 | 94 | 96 | PF00675 | 0.553 |
CLV_PCSK_KEX2_1 | 323 | 325 | PF00082 | 0.824 |
CLV_PCSK_KEX2_1 | 94 | 96 | PF00082 | 0.531 |
CLV_PCSK_SKI1_1 | 382 | 386 | PF00082 | 0.555 |
CLV_PCSK_SKI1_1 | 404 | 408 | PF00082 | 0.464 |
CLV_PCSK_SKI1_1 | 422 | 426 | PF00082 | 0.445 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.466 |
DEG_SPOP_SBC_1 | 180 | 184 | PF00917 | 0.446 |
DEG_SPOP_SBC_1 | 192 | 196 | PF00917 | 0.496 |
DOC_CYCLIN_RxL_1 | 109 | 120 | PF00134 | 0.503 |
DOC_CYCLIN_RxL_1 | 368 | 380 | PF00134 | 0.452 |
DOC_CYCLIN_RxL_1 | 419 | 429 | PF00134 | 0.453 |
DOC_CYCLIN_yCln2_LP_2 | 70 | 76 | PF00134 | 0.471 |
DOC_MAPK_MEF2A_6 | 431 | 438 | PF00069 | 0.303 |
DOC_PP1_RVXF_1 | 371 | 378 | PF00149 | 0.435 |
DOC_PP2B_LxvP_1 | 114 | 117 | PF13499 | 0.482 |
DOC_PP2B_LxvP_1 | 150 | 153 | PF13499 | 0.539 |
DOC_PP2B_LxvP_1 | 251 | 254 | PF13499 | 0.656 |
DOC_PP4_FxxP_1 | 237 | 240 | PF00568 | 0.468 |
DOC_USP7_MATH_1 | 117 | 121 | PF00917 | 0.629 |
DOC_USP7_MATH_1 | 206 | 210 | PF00917 | 0.452 |
DOC_USP7_MATH_1 | 254 | 258 | PF00917 | 0.751 |
DOC_USP7_MATH_1 | 286 | 290 | PF00917 | 0.750 |
DOC_USP7_MATH_1 | 314 | 318 | PF00917 | 0.712 |
DOC_USP7_MATH_1 | 340 | 344 | PF00917 | 0.401 |
DOC_USP7_MATH_1 | 352 | 356 | PF00917 | 0.464 |
DOC_USP7_MATH_1 | 49 | 53 | PF00917 | 0.654 |
DOC_WW_Pin1_4 | 16 | 21 | PF00397 | 0.410 |
DOC_WW_Pin1_4 | 268 | 273 | PF00397 | 0.724 |
DOC_WW_Pin1_4 | 416 | 421 | PF00397 | 0.505 |
LIG_14-3-3_CanoR_1 | 179 | 189 | PF00244 | 0.443 |
LIG_14-3-3_CanoR_1 | 208 | 213 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 229 | 235 | PF00244 | 0.546 |
LIG_BRCT_BRCA1_1 | 14 | 18 | PF00533 | 0.432 |
LIG_BRCT_BRCA1_1 | 288 | 292 | PF00533 | 0.682 |
LIG_BRCT_BRCA1_1 | 354 | 358 | PF00533 | 0.400 |
LIG_CSL_BTD_1 | 114 | 117 | PF09270 | 0.488 |
LIG_FHA_1 | 180 | 186 | PF00498 | 0.474 |
LIG_FHA_1 | 193 | 199 | PF00498 | 0.462 |
LIG_FHA_1 | 37 | 43 | PF00498 | 0.437 |
LIG_FHA_1 | 398 | 404 | PF00498 | 0.546 |
LIG_FHA_1 | 441 | 447 | PF00498 | 0.645 |
LIG_FHA_1 | 8 | 14 | PF00498 | 0.415 |
LIG_FHA_2 | 171 | 177 | PF00498 | 0.473 |
LIG_FHA_2 | 182 | 188 | PF00498 | 0.450 |
LIG_FHA_2 | 198 | 204 | PF00498 | 0.420 |
LIG_FHA_2 | 231 | 237 | PF00498 | 0.557 |
LIG_FHA_2 | 32 | 38 | PF00498 | 0.378 |
LIG_FHA_2 | 383 | 389 | PF00498 | 0.430 |
LIG_FHA_2 | 425 | 431 | PF00498 | 0.427 |
LIG_FHA_2 | 79 | 85 | PF00498 | 0.517 |
LIG_IBAR_NPY_1 | 75 | 77 | PF08397 | 0.426 |
LIG_LIR_Apic_2 | 235 | 240 | PF02991 | 0.482 |
LIG_LIR_Gen_1 | 133 | 139 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 133 | 137 | PF02991 | 0.431 |
LIG_PCNA_yPIPBox_3 | 102 | 114 | PF02747 | 0.370 |
LIG_Pex14_1 | 437 | 441 | PF04695 | 0.451 |
LIG_Pex14_2 | 347 | 351 | PF04695 | 0.466 |
LIG_SH2_CRK | 77 | 81 | PF00017 | 0.537 |
LIG_SH2_SRC | 146 | 149 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 146 | 149 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 371 | 374 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 77 | 80 | PF00017 | 0.537 |
LIG_SH3_3 | 163 | 169 | PF00018 | 0.509 |
LIG_SH3_3 | 186 | 192 | PF00018 | 0.438 |
LIG_SH3_3 | 242 | 248 | PF00018 | 0.503 |
LIG_SH3_3 | 70 | 76 | PF00018 | 0.426 |
LIG_SUMO_SIM_par_1 | 382 | 391 | PF11976 | 0.436 |
LIG_WW_3 | 320 | 324 | PF00397 | 0.571 |
MOD_CDC14_SPxK_1 | 419 | 422 | PF00782 | 0.607 |
MOD_CDK_SPxK_1 | 416 | 422 | PF00069 | 0.582 |
MOD_CK1_1 | 135 | 141 | PF00069 | 0.429 |
MOD_CK1_1 | 181 | 187 | PF00069 | 0.439 |
MOD_CK1_1 | 266 | 272 | PF00069 | 0.824 |
MOD_CK1_1 | 387 | 393 | PF00069 | 0.464 |
MOD_CK1_1 | 416 | 422 | PF00069 | 0.510 |
MOD_CK2_1 | 152 | 158 | PF00069 | 0.719 |
MOD_CK2_1 | 197 | 203 | PF00069 | 0.418 |
MOD_CK2_1 | 230 | 236 | PF00069 | 0.532 |
MOD_CK2_1 | 388 | 394 | PF00069 | 0.445 |
MOD_GlcNHglycan | 119 | 122 | PF01048 | 0.666 |
MOD_GlcNHglycan | 137 | 140 | PF01048 | 0.381 |
MOD_GlcNHglycan | 154 | 157 | PF01048 | 0.609 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.700 |
MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.793 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.445 |
MOD_GlcNHglycan | 354 | 357 | PF01048 | 0.408 |
MOD_GlcNHglycan | 415 | 418 | PF01048 | 0.421 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.372 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.681 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.581 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.466 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.541 |
MOD_GSK3_1 | 264 | 271 | PF00069 | 0.667 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.435 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.462 |
MOD_GSK3_1 | 384 | 391 | PF00069 | 0.457 |
MOD_GSK3_1 | 412 | 419 | PF00069 | 0.458 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.491 |
MOD_N-GLC_1 | 302 | 307 | PF02516 | 0.560 |
MOD_NEK2_1 | 178 | 183 | PF00069 | 0.453 |
MOD_NEK2_1 | 212 | 217 | PF00069 | 0.603 |
MOD_NEK2_1 | 264 | 269 | PF00069 | 0.569 |
MOD_NEK2_1 | 30 | 35 | PF00069 | 0.425 |
MOD_NEK2_1 | 412 | 417 | PF00069 | 0.482 |
MOD_NEK2_1 | 424 | 429 | PF00069 | 0.470 |
MOD_NEK2_2 | 287 | 292 | PF00069 | 0.506 |
MOD_PIKK_1 | 254 | 260 | PF00454 | 0.510 |
MOD_PIKK_1 | 49 | 55 | PF00454 | 0.581 |
MOD_PKA_2 | 178 | 184 | PF00069 | 0.503 |
MOD_PKA_2 | 212 | 218 | PF00069 | 0.568 |
MOD_Plk_1 | 132 | 138 | PF00069 | 0.343 |
MOD_Plk_1 | 388 | 394 | PF00069 | 0.445 |
MOD_Plk_1 | 84 | 90 | PF00069 | 0.517 |
MOD_Plk_4 | 12 | 18 | PF00069 | 0.414 |
MOD_Plk_4 | 170 | 176 | PF00069 | 0.402 |
MOD_Plk_4 | 193 | 199 | PF00069 | 0.413 |
MOD_Plk_4 | 287 | 293 | PF00069 | 0.503 |
MOD_Plk_4 | 75 | 81 | PF00069 | 0.607 |
MOD_ProDKin_1 | 16 | 22 | PF00069 | 0.419 |
MOD_ProDKin_1 | 268 | 274 | PF00069 | 0.724 |
MOD_ProDKin_1 | 416 | 422 | PF00069 | 0.510 |
MOD_SUMO_rev_2 | 376 | 384 | PF00179 | 0.577 |
TRG_DiLeu_BaLyEn_6 | 226 | 231 | PF01217 | 0.571 |
TRG_ENDOCYTIC_2 | 77 | 80 | PF00928 | 0.584 |
TRG_ER_diArg_1 | 322 | 324 | PF00400 | 0.829 |
TRG_ER_diArg_1 | 93 | 95 | PF00400 | 0.546 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IM43 | Leptomonas seymouri | 67% | 100% |
A0A3S7WX82 | Leishmania donovani | 83% | 100% |
A0A422N3N4 | Trypanosoma rangeli | 33% | 100% |
E9AGZ5 | Leishmania infantum | 83% | 100% |
E9AVV7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
Q4QBM2 | Leishmania major | 85% | 100% |