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 | 1 |
GO:0005930 | axoneme | 2 | 1 |
GO:0031974 | membrane-enclosed lumen | 2 | 1 |
GO:0031981 | nuclear lumen | 5 | 1 |
GO:0043233 | organelle lumen | 3 | 1 |
GO:0070013 | intracellular organelle lumen | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AU52
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 123 | 125 | PF00675 | 0.708 |
CLV_PCSK_KEX2_1 | 123 | 125 | PF00082 | 0.708 |
CLV_PCSK_KEX2_1 | 22 | 24 | PF00082 | 0.807 |
CLV_PCSK_KEX2_1 | 478 | 480 | PF00082 | 0.791 |
CLV_PCSK_PC1ET2_1 | 22 | 24 | PF00082 | 0.807 |
CLV_PCSK_PC1ET2_1 | 478 | 480 | PF00082 | 0.791 |
CLV_PCSK_SKI1_1 | 442 | 446 | PF00082 | 0.589 |
DEG_SPOP_SBC_1 | 34 | 38 | PF00917 | 0.409 |
DEG_SPOP_SBC_1 | 40 | 44 | PF00917 | 0.338 |
DOC_CKS1_1 | 352 | 357 | PF01111 | 0.397 |
DOC_CYCLIN_RxL_1 | 439 | 449 | PF00134 | 0.674 |
DOC_MAPK_gen_1 | 169 | 179 | PF00069 | 0.347 |
DOC_MAPK_MEF2A_6 | 261 | 270 | PF00069 | 0.341 |
DOC_MAPK_MEF2A_6 | 461 | 469 | PF00069 | 0.747 |
DOC_PP1_RVXF_1 | 440 | 447 | PF00149 | 0.670 |
DOC_PP4_FxxP_1 | 195 | 198 | PF00568 | 0.346 |
DOC_USP7_MATH_1 | 211 | 215 | PF00917 | 0.643 |
DOC_USP7_MATH_1 | 224 | 228 | PF00917 | 0.532 |
DOC_USP7_MATH_1 | 376 | 380 | PF00917 | 0.723 |
DOC_USP7_MATH_1 | 410 | 414 | PF00917 | 0.730 |
DOC_USP7_MATH_1 | 415 | 419 | PF00917 | 0.757 |
DOC_USP7_MATH_1 | 89 | 93 | PF00917 | 0.499 |
DOC_USP7_MATH_1 | 98 | 102 | PF00917 | 0.519 |
DOC_USP7_UBL2_3 | 18 | 22 | PF12436 | 0.795 |
DOC_WW_Pin1_4 | 133 | 138 | PF00397 | 0.718 |
DOC_WW_Pin1_4 | 148 | 153 | PF00397 | 0.572 |
DOC_WW_Pin1_4 | 16 | 21 | PF00397 | 0.571 |
DOC_WW_Pin1_4 | 202 | 207 | PF00397 | 0.676 |
DOC_WW_Pin1_4 | 278 | 283 | PF00397 | 0.408 |
DOC_WW_Pin1_4 | 332 | 337 | PF00397 | 0.570 |
DOC_WW_Pin1_4 | 351 | 356 | PF00397 | 0.383 |
LIG_14-3-3_CanoR_1 | 147 | 152 | PF00244 | 0.724 |
LIG_14-3-3_CanoR_1 | 156 | 164 | PF00244 | 0.715 |
LIG_14-3-3_CanoR_1 | 178 | 184 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 201 | 206 | PF00244 | 0.627 |
LIG_14-3-3_CanoR_1 | 23 | 33 | PF00244 | 0.759 |
LIG_14-3-3_CanoR_1 | 349 | 355 | PF00244 | 0.545 |
LIG_14-3-3_CanoR_1 | 392 | 401 | PF00244 | 0.608 |
LIG_14-3-3_CanoR_1 | 414 | 420 | PF00244 | 0.766 |
LIG_Actin_WH2_2 | 265 | 281 | PF00022 | 0.579 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.610 |
LIG_CSL_BTD_1 | 333 | 336 | PF09270 | 0.580 |
LIG_CtBP_PxDLS_1 | 137 | 141 | PF00389 | 0.797 |
LIG_deltaCOP1_diTrp_1 | 258 | 263 | PF00928 | 0.539 |
LIG_FHA_1 | 251 | 257 | PF00498 | 0.553 |
LIG_FHA_1 | 279 | 285 | PF00498 | 0.417 |
LIG_FHA_1 | 310 | 316 | PF00498 | 0.590 |
LIG_FHA_1 | 34 | 40 | PF00498 | 0.599 |
LIG_FHA_1 | 59 | 65 | PF00498 | 0.623 |
LIG_FHA_2 | 236 | 242 | PF00498 | 0.663 |
LIG_LIR_Gen_1 | 2 | 13 | PF02991 | 0.491 |
LIG_LIR_Gen_1 | 367 | 376 | PF02991 | 0.616 |
LIG_LIR_Gen_1 | 75 | 86 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 2 | 8 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 333 | 337 | PF02991 | 0.576 |
LIG_LIR_Nem_3 | 367 | 372 | PF02991 | 0.493 |
LIG_LIR_Nem_3 | 430 | 435 | PF02991 | 0.707 |
LIG_LIR_Nem_3 | 75 | 81 | PF02991 | 0.461 |
LIG_NRP_CendR_1 | 483 | 485 | PF00754 | 0.808 |
LIG_Pex14_1 | 334 | 338 | PF04695 | 0.582 |
LIG_SH2_CRK | 5 | 9 | PF00017 | 0.489 |
LIG_SH2_NCK_1 | 13 | 17 | PF00017 | 0.775 |
LIG_SH2_SRC | 13 | 16 | PF00017 | 0.775 |
LIG_SH2_STAP1 | 13 | 17 | PF00017 | 0.775 |
LIG_SH2_STAP1 | 164 | 168 | PF00017 | 0.425 |
LIG_SH2_STAP1 | 67 | 71 | PF00017 | 0.573 |
LIG_SH2_STAT5 | 245 | 248 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 369 | 372 | PF00017 | 0.435 |
LIG_SH3_2 | 82 | 87 | PF14604 | 0.608 |
LIG_SH3_3 | 119 | 125 | PF00018 | 0.488 |
LIG_SH3_3 | 131 | 137 | PF00018 | 0.674 |
LIG_SH3_3 | 203 | 209 | PF00018 | 0.636 |
LIG_SH3_3 | 28 | 34 | PF00018 | 0.662 |
LIG_SH3_3 | 333 | 339 | PF00018 | 0.506 |
LIG_SH3_3 | 352 | 358 | PF00018 | 0.343 |
LIG_SH3_3 | 79 | 85 | PF00018 | 0.498 |
LIG_TYR_ITIM | 65 | 70 | PF00017 | 0.567 |
LIG_UBA3_1 | 444 | 448 | PF00899 | 0.405 |
MOD_CDC14_SPxK_1 | 19 | 22 | PF00782 | 0.524 |
MOD_CDK_SPxK_1 | 16 | 22 | PF00069 | 0.520 |
MOD_CDK_SPxxK_3 | 16 | 23 | PF00069 | 0.520 |
MOD_CK1_1 | 136 | 142 | PF00069 | 0.796 |
MOD_CK1_1 | 196 | 202 | PF00069 | 0.482 |
MOD_CK1_1 | 205 | 211 | PF00069 | 0.794 |
MOD_CK1_1 | 309 | 315 | PF00069 | 0.589 |
MOD_CK1_1 | 327 | 333 | PF00069 | 0.596 |
MOD_CK1_1 | 413 | 419 | PF00069 | 0.792 |
MOD_CK2_1 | 235 | 241 | PF00069 | 0.685 |
MOD_CK2_1 | 35 | 41 | PF00069 | 0.496 |
MOD_CK2_1 | 4 | 10 | PF00069 | 0.759 |
MOD_CMANNOS | 260 | 263 | PF00535 | 0.536 |
MOD_GlcNHglycan | 113 | 116 | PF01048 | 0.357 |
MOD_GlcNHglycan | 130 | 133 | PF01048 | 0.619 |
MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.640 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.557 |
MOD_GlcNHglycan | 195 | 198 | PF01048 | 0.367 |
MOD_GlcNHglycan | 217 | 220 | PF01048 | 0.736 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.644 |
MOD_GlcNHglycan | 231 | 234 | PF01048 | 0.620 |
MOD_GlcNHglycan | 329 | 332 | PF01048 | 0.604 |
MOD_GlcNHglycan | 449 | 452 | PF01048 | 0.605 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.555 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.691 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.681 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.734 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.668 |
MOD_GSK3_1 | 409 | 416 | PF00069 | 0.696 |
MOD_GSK3_1 | 453 | 460 | PF00069 | 0.701 |
MOD_GSK3_1 | 474 | 481 | PF00069 | 0.726 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.463 |
MOD_N-GLC_1 | 249 | 254 | PF02516 | 0.580 |
MOD_N-GLC_1 | 350 | 355 | PF02516 | 0.699 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.606 |
MOD_NEK2_1 | 393 | 398 | PF00069 | 0.511 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.487 |
MOD_NEK2_1 | 419 | 424 | PF00069 | 0.555 |
MOD_NEK2_1 | 447 | 452 | PF00069 | 0.597 |
MOD_NEK2_1 | 471 | 476 | PF00069 | 0.725 |
MOD_NEK2_2 | 415 | 420 | PF00069 | 0.800 |
MOD_PIKK_1 | 24 | 30 | PF00454 | 0.665 |
MOD_PIKK_1 | 455 | 461 | PF00454 | 0.787 |
MOD_PIKK_1 | 58 | 64 | PF00454 | 0.534 |
MOD_PKA_1 | 478 | 484 | PF00069 | 0.526 |
MOD_PKA_2 | 146 | 152 | PF00069 | 0.726 |
MOD_PKA_2 | 157 | 163 | PF00069 | 0.710 |
MOD_PKA_2 | 177 | 183 | PF00069 | 0.329 |
MOD_PKA_2 | 386 | 392 | PF00069 | 0.373 |
MOD_PKA_2 | 413 | 419 | PF00069 | 0.759 |
MOD_PKA_2 | 478 | 484 | PF00069 | 0.526 |
MOD_Plk_1 | 325 | 331 | PF00069 | 0.528 |
MOD_Plk_1 | 40 | 46 | PF00069 | 0.615 |
MOD_Plk_4 | 226 | 232 | PF00069 | 0.755 |
MOD_Plk_4 | 319 | 325 | PF00069 | 0.573 |
MOD_Plk_4 | 35 | 41 | PF00069 | 0.496 |
MOD_Plk_4 | 364 | 370 | PF00069 | 0.492 |
MOD_Plk_4 | 386 | 392 | PF00069 | 0.373 |
MOD_Plk_4 | 98 | 104 | PF00069 | 0.603 |
MOD_ProDKin_1 | 133 | 139 | PF00069 | 0.719 |
MOD_ProDKin_1 | 148 | 154 | PF00069 | 0.574 |
MOD_ProDKin_1 | 16 | 22 | PF00069 | 0.574 |
MOD_ProDKin_1 | 202 | 208 | PF00069 | 0.682 |
MOD_ProDKin_1 | 278 | 284 | PF00069 | 0.410 |
MOD_ProDKin_1 | 332 | 338 | PF00069 | 0.579 |
MOD_ProDKin_1 | 351 | 357 | PF00069 | 0.371 |
MOD_SUMO_rev_2 | 402 | 411 | PF00179 | 0.457 |
MOD_SUMO_rev_2 | 468 | 477 | PF00179 | 0.667 |
TRG_DiLeu_BaEn_2 | 47 | 53 | PF01217 | 0.605 |
TRG_ENDOCYTIC_2 | 369 | 372 | PF00928 | 0.498 |
TRG_ENDOCYTIC_2 | 5 | 8 | PF00928 | 0.545 |
TRG_ENDOCYTIC_2 | 67 | 70 | PF00928 | 0.573 |
TRG_ER_diArg_1 | 122 | 124 | PF00400 | 0.661 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7XC07 | Leishmania donovani | 83% | 100% |
A4IE28 | Leishmania infantum | 83% | 100% |
D0A3W0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
Q4Q0E3 | Leishmania major | 84% | 100% |