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:0005737 | cytoplasm | 2 | 2 |
GO:0005930 | axoneme | 2 | 2 |
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: Q4Q0E3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 123 | 125 | PF00675 | 0.714 |
CLV_NRD_NRD_1 | 479 | 481 | PF00675 | 0.723 |
CLV_PCSK_KEX2_1 | 123 | 125 | PF00082 | 0.714 |
CLV_PCSK_KEX2_1 | 22 | 24 | PF00082 | 0.806 |
CLV_PCSK_KEX2_1 | 478 | 480 | PF00082 | 0.826 |
CLV_PCSK_PC1ET2_1 | 22 | 24 | PF00082 | 0.806 |
CLV_PCSK_PC1ET2_1 | 478 | 480 | PF00082 | 0.826 |
CLV_PCSK_SKI1_1 | 442 | 446 | PF00082 | 0.555 |
DEG_SCF_FBW7_1 | 332 | 339 | PF00400 | 0.330 |
DOC_CKS1_1 | 263 | 268 | PF01111 | 0.509 |
DOC_CYCLIN_RxL_1 | 439 | 449 | PF00134 | 0.658 |
DOC_MAPK_DCC_7 | 134 | 142 | PF00069 | 0.770 |
DOC_MAPK_MEF2A_6 | 134 | 142 | PF00069 | 0.770 |
DOC_MAPK_MEF2A_6 | 461 | 469 | PF00069 | 0.729 |
DOC_PP1_RVXF_1 | 440 | 447 | PF00149 | 0.650 |
DOC_USP7_MATH_1 | 16 | 20 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 199 | 203 | PF00917 | 0.756 |
DOC_USP7_MATH_1 | 376 | 380 | PF00917 | 0.724 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.714 |
DOC_USP7_MATH_1 | 410 | 414 | PF00917 | 0.723 |
DOC_USP7_MATH_1 | 415 | 419 | PF00917 | 0.745 |
DOC_USP7_MATH_1 | 481 | 485 | PF00917 | 0.756 |
DOC_USP7_MATH_1 | 89 | 93 | PF00917 | 0.601 |
DOC_USP7_MATH_1 | 98 | 102 | PF00917 | 0.488 |
DOC_USP7_UBL2_3 | 18 | 22 | PF12436 | 0.787 |
DOC_WW_Pin1_4 | 133 | 138 | PF00397 | 0.750 |
DOC_WW_Pin1_4 | 148 | 153 | PF00397 | 0.593 |
DOC_WW_Pin1_4 | 206 | 211 | PF00397 | 0.797 |
DOC_WW_Pin1_4 | 233 | 238 | PF00397 | 0.698 |
DOC_WW_Pin1_4 | 262 | 267 | PF00397 | 0.505 |
DOC_WW_Pin1_4 | 278 | 283 | PF00397 | 0.563 |
DOC_WW_Pin1_4 | 332 | 337 | PF00397 | 0.560 |
LIG_14-3-3_CanoR_1 | 147 | 152 | PF00244 | 0.745 |
LIG_14-3-3_CanoR_1 | 178 | 184 | PF00244 | 0.545 |
LIG_14-3-3_CanoR_1 | 23 | 27 | PF00244 | 0.799 |
LIG_14-3-3_CanoR_1 | 349 | 359 | PF00244 | 0.484 |
LIG_14-3-3_CanoR_1 | 392 | 401 | PF00244 | 0.583 |
LIG_14-3-3_CanoR_1 | 420 | 424 | PF00244 | 0.715 |
LIG_14-3-3_CanoR_1 | 433 | 443 | PF00244 | 0.379 |
LIG_Actin_WH2_2 | 265 | 281 | PF00022 | 0.594 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.680 |
LIG_BIR_III_1 | 1 | 5 | PF00653 | 0.714 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.714 |
LIG_CSL_BTD_1 | 333 | 336 | PF09270 | 0.569 |
LIG_CtBP_PxDLS_1 | 137 | 141 | PF00389 | 0.825 |
LIG_deltaCOP1_diTrp_1 | 258 | 263 | PF00928 | 0.557 |
LIG_FHA_1 | 251 | 257 | PF00498 | 0.513 |
LIG_FHA_1 | 263 | 269 | PF00498 | 0.541 |
LIG_FHA_1 | 279 | 285 | PF00498 | 0.639 |
LIG_FHA_1 | 310 | 316 | PF00498 | 0.581 |
LIG_FHA_1 | 34 | 40 | PF00498 | 0.670 |
LIG_FHA_1 | 59 | 65 | PF00498 | 0.503 |
LIG_FHA_2 | 152 | 158 | PF00498 | 0.632 |
LIG_FHA_2 | 236 | 242 | PF00498 | 0.674 |
LIG_Integrin_isoDGR_2 | 385 | 387 | PF01839 | 0.663 |
LIG_LIR_Gen_1 | 367 | 376 | PF02991 | 0.599 |
LIG_LIR_Gen_1 | 75 | 86 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 241 | 247 | PF02991 | 0.337 |
LIG_LIR_Nem_3 | 333 | 337 | PF02991 | 0.565 |
LIG_LIR_Nem_3 | 367 | 372 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 430 | 435 | PF02991 | 0.681 |
LIG_LIR_Nem_3 | 75 | 81 | PF02991 | 0.341 |
LIG_LYPXL_SIV_4 | 12 | 20 | PF13949 | 0.724 |
LIG_NRP_CendR_1 | 483 | 485 | PF00754 | 0.838 |
LIG_Pex14_1 | 334 | 338 | PF04695 | 0.572 |
LIG_SH2_NCK_1 | 13 | 17 | PF00017 | 0.776 |
LIG_SH2_SRC | 13 | 16 | PF00017 | 0.778 |
LIG_SH2_STAP1 | 13 | 17 | PF00017 | 0.776 |
LIG_SH2_STAP1 | 67 | 71 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 245 | 248 | PF00017 | 0.465 |
LIG_SH2_STAT5 | 369 | 372 | PF00017 | 0.476 |
LIG_SH3_2 | 82 | 87 | PF14604 | 0.612 |
LIG_SH3_3 | 132 | 138 | PF00018 | 0.770 |
LIG_SH3_3 | 192 | 198 | PF00018 | 0.599 |
LIG_SH3_3 | 204 | 210 | PF00018 | 0.666 |
LIG_SH3_3 | 79 | 85 | PF00018 | 0.406 |
LIG_TYR_ITIM | 65 | 70 | PF00017 | 0.503 |
LIG_WRC_WIRS_1 | 429 | 434 | PF05994 | 0.478 |
MOD_CK1_1 | 136 | 142 | PF00069 | 0.823 |
MOD_CK1_1 | 309 | 315 | PF00069 | 0.577 |
MOD_CK1_1 | 327 | 333 | PF00069 | 0.432 |
MOD_CK1_1 | 413 | 419 | PF00069 | 0.781 |
MOD_CK1_1 | 471 | 477 | PF00069 | 0.576 |
MOD_CK2_1 | 151 | 157 | PF00069 | 0.728 |
MOD_CK2_1 | 235 | 241 | PF00069 | 0.695 |
MOD_CK2_1 | 35 | 41 | PF00069 | 0.497 |
MOD_CK2_1 | 4 | 10 | PF00069 | 0.771 |
MOD_CMANNOS | 260 | 263 | PF00535 | 0.556 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.518 |
MOD_GlcNHglycan | 195 | 198 | PF01048 | 0.430 |
MOD_GlcNHglycan | 231 | 234 | PF01048 | 0.684 |
MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.555 |
MOD_GlcNHglycan | 329 | 332 | PF01048 | 0.373 |
MOD_GlcNHglycan | 449 | 452 | PF01048 | 0.577 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.597 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.798 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.836 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.806 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.808 |
MOD_GSK3_1 | 229 | 236 | PF00069 | 0.567 |
MOD_GSK3_1 | 332 | 339 | PF00069 | 0.330 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.635 |
MOD_GSK3_1 | 409 | 416 | PF00069 | 0.689 |
MOD_GSK3_1 | 453 | 460 | PF00069 | 0.787 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.348 |
MOD_N-GLC_1 | 249 | 254 | PF02516 | 0.583 |
MOD_N-GLC_1 | 350 | 355 | PF02516 | 0.681 |
MOD_NEK2_1 | 140 | 145 | PF00069 | 0.783 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.539 |
MOD_NEK2_1 | 393 | 398 | PF00069 | 0.485 |
MOD_NEK2_1 | 40 | 45 | PF00069 | 0.427 |
MOD_NEK2_1 | 401 | 406 | PF00069 | 0.573 |
MOD_NEK2_1 | 419 | 424 | PF00069 | 0.539 |
MOD_NEK2_1 | 447 | 452 | PF00069 | 0.677 |
MOD_NEK2_2 | 226 | 231 | PF00069 | 0.763 |
MOD_NEK2_2 | 415 | 420 | PF00069 | 0.788 |
MOD_PIKK_1 | 199 | 205 | PF00454 | 0.746 |
MOD_PIKK_1 | 410 | 416 | PF00454 | 0.555 |
MOD_PIKK_1 | 455 | 461 | PF00454 | 0.787 |
MOD_PIKK_1 | 58 | 64 | PF00454 | 0.428 |
MOD_PKA_1 | 22 | 28 | PF00069 | 0.744 |
MOD_PKA_2 | 146 | 152 | PF00069 | 0.748 |
MOD_PKA_2 | 157 | 163 | PF00069 | 0.738 |
MOD_PKA_2 | 177 | 183 | PF00069 | 0.345 |
MOD_PKA_2 | 22 | 28 | PF00069 | 0.744 |
MOD_PKA_2 | 419 | 425 | PF00069 | 0.714 |
MOD_Plk_1 | 40 | 46 | PF00069 | 0.503 |
MOD_Plk_2-3 | 468 | 474 | PF00069 | 0.538 |
MOD_Plk_4 | 226 | 232 | PF00069 | 0.779 |
MOD_Plk_4 | 319 | 325 | PF00069 | 0.526 |
MOD_Plk_4 | 35 | 41 | PF00069 | 0.497 |
MOD_Plk_4 | 364 | 370 | PF00069 | 0.574 |
MOD_Plk_4 | 98 | 104 | PF00069 | 0.613 |
MOD_ProDKin_1 | 133 | 139 | PF00069 | 0.751 |
MOD_ProDKin_1 | 148 | 154 | PF00069 | 0.593 |
MOD_ProDKin_1 | 206 | 212 | PF00069 | 0.798 |
MOD_ProDKin_1 | 233 | 239 | PF00069 | 0.685 |
MOD_ProDKin_1 | 262 | 268 | PF00069 | 0.508 |
MOD_ProDKin_1 | 278 | 284 | PF00069 | 0.563 |
MOD_ProDKin_1 | 332 | 338 | PF00069 | 0.569 |
MOD_SUMO_rev_2 | 42 | 52 | PF00179 | 0.392 |
MOD_SUMO_rev_2 | 468 | 477 | PF00179 | 0.716 |
TRG_DiLeu_BaEn_2 | 47 | 53 | PF01217 | 0.503 |
TRG_ENDOCYTIC_2 | 369 | 372 | PF00928 | 0.476 |
TRG_ENDOCYTIC_2 | 67 | 70 | PF00928 | 0.503 |
TRG_ER_diArg_1 | 122 | 124 | PF00400 | 0.679 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7XC07 | Leishmania donovani | 89% | 100% |
A4IE28 | Leishmania infantum | 90% | 100% |
D0A3W0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
E9AU52 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |