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: 20 |
NetGPI | no | yes: 0, no: 20 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005739 | mitochondrion | 5 | 1 |
GO:0020023 | kinetoplast | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4H889
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 274 | 278 | PF00656 | 0.478 |
CLV_C14_Caspase3-7 | 415 | 419 | PF00656 | 0.453 |
CLV_NRD_NRD_1 | 305 | 307 | PF00675 | 0.401 |
CLV_NRD_NRD_1 | 376 | 378 | PF00675 | 0.554 |
CLV_NRD_NRD_1 | 70 | 72 | PF00675 | 0.401 |
CLV_NRD_NRD_1 | 89 | 91 | PF00675 | 0.382 |
CLV_PCSK_KEX2_1 | 376 | 378 | PF00082 | 0.615 |
CLV_PCSK_KEX2_1 | 380 | 382 | PF00082 | 0.622 |
CLV_PCSK_KEX2_1 | 44 | 46 | PF00082 | 0.405 |
CLV_PCSK_KEX2_1 | 474 | 476 | PF00082 | 0.784 |
CLV_PCSK_KEX2_1 | 89 | 91 | PF00082 | 0.485 |
CLV_PCSK_PC1ET2_1 | 380 | 382 | PF00082 | 0.539 |
CLV_PCSK_PC1ET2_1 | 44 | 46 | PF00082 | 0.420 |
CLV_PCSK_PC1ET2_1 | 474 | 476 | PF00082 | 0.769 |
CLV_PCSK_PC7_1 | 376 | 382 | PF00082 | 0.405 |
CLV_PCSK_SKI1_1 | 215 | 219 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 291 | 295 | PF00082 | 0.566 |
CLV_PCSK_SKI1_1 | 307 | 311 | PF00082 | 0.293 |
CLV_PCSK_SKI1_1 | 312 | 316 | PF00082 | 0.336 |
CLV_PCSK_SKI1_1 | 319 | 323 | PF00082 | 0.392 |
CLV_PCSK_SKI1_1 | 377 | 381 | PF00082 | 0.586 |
DEG_APCC_DBOX_1 | 123 | 131 | PF00400 | 0.445 |
DEG_APCC_DBOX_1 | 311 | 319 | PF00400 | 0.363 |
DEG_SPOP_SBC_1 | 235 | 239 | PF00917 | 0.473 |
DEG_SPOP_SBC_1 | 257 | 261 | PF00917 | 0.651 |
DEG_SPOP_SBC_1 | 270 | 274 | PF00917 | 0.553 |
DOC_CYCLIN_RxL_1 | 316 | 325 | PF00134 | 0.381 |
DOC_CYCLIN_yClb1_LxF_4 | 189 | 195 | PF00134 | 0.321 |
DOC_MAPK_FxFP_2 | 332 | 335 | PF00069 | 0.544 |
DOC_MAPK_gen_1 | 71 | 79 | PF00069 | 0.449 |
DOC_MAPK_MEF2A_6 | 364 | 372 | PF00069 | 0.600 |
DOC_PP2B_LxvP_1 | 21 | 24 | PF13499 | 0.536 |
DOC_PP2B_LxvP_1 | 321 | 324 | PF13499 | 0.405 |
DOC_PP4_FxxP_1 | 332 | 335 | PF00568 | 0.544 |
DOC_PP4_FxxP_1 | 49 | 52 | PF00568 | 0.449 |
DOC_USP7_MATH_1 | 236 | 240 | PF00917 | 0.533 |
DOC_USP7_MATH_1 | 255 | 259 | PF00917 | 0.603 |
DOC_USP7_MATH_1 | 263 | 267 | PF00917 | 0.751 |
DOC_USP7_MATH_1 | 271 | 275 | PF00917 | 0.689 |
DOC_USP7_MATH_1 | 455 | 459 | PF00917 | 0.558 |
DOC_USP7_MATH_1 | 461 | 465 | PF00917 | 0.510 |
DOC_USP7_MATH_2 | 26 | 32 | PF00917 | 0.459 |
DOC_USP7_UBL2_3 | 294 | 298 | PF12436 | 0.475 |
DOC_WW_Pin1_4 | 223 | 228 | PF00397 | 0.508 |
LIG_14-3-3_CanoR_1 | 306 | 314 | PF00244 | 0.479 |
LIG_14-3-3_CanoR_1 | 396 | 400 | PF00244 | 0.589 |
LIG_14-3-3_CanoR_1 | 4 | 10 | PF00244 | 0.636 |
LIG_14-3-3_CanoR_1 | 475 | 481 | PF00244 | 0.489 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.443 |
LIG_Clathr_ClatBox_1 | 131 | 135 | PF01394 | 0.342 |
LIG_deltaCOP1_diTrp_1 | 366 | 372 | PF00928 | 0.509 |
LIG_deltaCOP1_diTrp_1 | 86 | 91 | PF00928 | 0.571 |
LIG_FHA_1 | 279 | 285 | PF00498 | 0.401 |
LIG_FHA_2 | 201 | 207 | PF00498 | 0.303 |
LIG_FHA_2 | 338 | 344 | PF00498 | 0.555 |
LIG_FHA_2 | 97 | 103 | PF00498 | 0.405 |
LIG_GBD_Chelix_1 | 350 | 358 | PF00786 | 0.368 |
LIG_LIR_Gen_1 | 110 | 119 | PF02991 | 0.612 |
LIG_LIR_Gen_1 | 125 | 134 | PF02991 | 0.233 |
LIG_LIR_Gen_1 | 187 | 195 | PF02991 | 0.331 |
LIG_LIR_Gen_1 | 366 | 374 | PF02991 | 0.455 |
LIG_LIR_Gen_1 | 78 | 88 | PF02991 | 0.384 |
LIG_LIR_Nem_3 | 110 | 115 | PF02991 | 0.523 |
LIG_LIR_Nem_3 | 125 | 131 | PF02991 | 0.241 |
LIG_LIR_Nem_3 | 187 | 191 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 366 | 372 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 78 | 84 | PF02991 | 0.410 |
LIG_NRBOX | 317 | 323 | PF00104 | 0.489 |
LIG_PCNA_yPIPBox_3 | 59 | 72 | PF02747 | 0.386 |
LIG_Pex14_2 | 176 | 180 | PF04695 | 0.484 |
LIG_SH2_CRK | 112 | 116 | PF00017 | 0.452 |
LIG_SH2_CRK | 128 | 132 | PF00017 | 0.314 |
LIG_SH2_CRK | 188 | 192 | PF00017 | 0.361 |
LIG_SH2_CRK | 81 | 85 | PF00017 | 0.408 |
LIG_SH2_GRB2like | 188 | 191 | PF00017 | 0.363 |
LIG_SH2_GRB2like | 245 | 248 | PF00017 | 0.493 |
LIG_SH2_STAP1 | 128 | 132 | PF00017 | 0.336 |
LIG_SH2_STAP1 | 188 | 192 | PF00017 | 0.361 |
LIG_SH2_STAP1 | 245 | 249 | PF00017 | 0.487 |
LIG_SH2_STAP1 | 81 | 85 | PF00017 | 0.365 |
LIG_SH2_STAT3 | 410 | 413 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 149 | 152 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 211 | 214 | PF00017 | 0.369 |
LIG_SH3_3 | 17 | 23 | PF00018 | 0.690 |
LIG_SH3_3 | 221 | 227 | PF00018 | 0.487 |
LIG_SUMO_SIM_par_1 | 337 | 343 | PF11976 | 0.415 |
LIG_SUMO_SIM_par_1 | 349 | 355 | PF11976 | 0.316 |
LIG_TRAF2_1 | 299 | 302 | PF00917 | 0.647 |
LIG_TRAF2_1 | 324 | 327 | PF00917 | 0.484 |
LIG_TYR_ITIM | 79 | 84 | PF00017 | 0.505 |
LIG_WRC_WIRS_1 | 97 | 102 | PF05994 | 0.590 |
MOD_CK1_1 | 145 | 151 | PF00069 | 0.537 |
MOD_CK1_1 | 239 | 245 | PF00069 | 0.549 |
MOD_CK1_1 | 258 | 264 | PF00069 | 0.690 |
MOD_CK1_1 | 278 | 284 | PF00069 | 0.496 |
MOD_CK1_1 | 305 | 311 | PF00069 | 0.467 |
MOD_CK1_1 | 470 | 476 | PF00069 | 0.681 |
MOD_CK2_1 | 296 | 302 | PF00069 | 0.682 |
MOD_CK2_1 | 337 | 343 | PF00069 | 0.474 |
MOD_CK2_1 | 96 | 102 | PF00069 | 0.608 |
MOD_GlcNHglycan | 239 | 242 | PF01048 | 0.522 |
MOD_GlcNHglycan | 260 | 263 | PF01048 | 0.703 |
MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.686 |
MOD_GlcNHglycan | 307 | 310 | PF01048 | 0.429 |
MOD_GlcNHglycan | 414 | 417 | PF01048 | 0.552 |
MOD_GlcNHglycan | 444 | 447 | PF01048 | 0.685 |
MOD_GlcNHglycan | 464 | 467 | PF01048 | 0.742 |
MOD_GlcNHglycan | 469 | 472 | PF01048 | 0.720 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.466 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.567 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.540 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.686 |
MOD_GSK3_1 | 265 | 272 | PF00069 | 0.678 |
MOD_GSK3_1 | 275 | 282 | PF00069 | 0.501 |
MOD_GSK3_1 | 408 | 415 | PF00069 | 0.698 |
MOD_GSK3_1 | 475 | 482 | PF00069 | 0.492 |
MOD_N-GLC_1 | 255 | 260 | PF02516 | 0.511 |
MOD_N-GLC_1 | 275 | 280 | PF02516 | 0.430 |
MOD_NEK2_1 | 195 | 200 | PF00069 | 0.318 |
MOD_NEK2_1 | 249 | 254 | PF00069 | 0.473 |
MOD_NEK2_1 | 409 | 414 | PF00069 | 0.546 |
MOD_NEK2_1 | 476 | 481 | PF00069 | 0.729 |
MOD_NEK2_1 | 79 | 84 | PF00069 | 0.413 |
MOD_PIKK_1 | 409 | 415 | PF00454 | 0.684 |
MOD_PIKK_1 | 79 | 85 | PF00454 | 0.357 |
MOD_PKA_2 | 145 | 151 | PF00069 | 0.387 |
MOD_PKA_2 | 305 | 311 | PF00069 | 0.543 |
MOD_PKA_2 | 395 | 401 | PF00069 | 0.531 |
MOD_PKA_2 | 461 | 467 | PF00069 | 0.657 |
MOD_PKA_2 | 5 | 11 | PF00069 | 0.657 |
MOD_PKB_1 | 460 | 468 | PF00069 | 0.634 |
MOD_Plk_4 | 145 | 151 | PF00069 | 0.438 |
MOD_Plk_4 | 200 | 206 | PF00069 | 0.313 |
MOD_Plk_4 | 33 | 39 | PF00069 | 0.567 |
MOD_Plk_4 | 476 | 482 | PF00069 | 0.488 |
MOD_Plk_4 | 96 | 102 | PF00069 | 0.487 |
MOD_ProDKin_1 | 223 | 229 | PF00069 | 0.510 |
MOD_SUMO_for_1 | 132 | 135 | PF00179 | 0.392 |
TRG_ENDOCYTIC_2 | 112 | 115 | PF00928 | 0.621 |
TRG_ENDOCYTIC_2 | 128 | 131 | PF00928 | 0.330 |
TRG_ENDOCYTIC_2 | 188 | 191 | PF00928 | 0.362 |
TRG_ENDOCYTIC_2 | 35 | 38 | PF00928 | 0.577 |
TRG_ENDOCYTIC_2 | 399 | 402 | PF00928 | 0.508 |
TRG_ENDOCYTIC_2 | 81 | 84 | PF00928 | 0.348 |
TRG_ER_diArg_1 | 4 | 7 | PF00400 | 0.645 |
TRG_ER_diArg_1 | 460 | 463 | PF00400 | 0.644 |
TRG_ER_diArg_1 | 88 | 90 | PF00400 | 0.450 |
TRG_NES_CRM1_1 | 313 | 327 | PF08389 | 0.377 |
TRG_NLS_MonoExtC_3 | 426 | 431 | PF00514 | 0.425 |
TRG_Pf-PMV_PEXEL_1 | 312 | 317 | PF00026 | 0.295 |
TRG_Pf-PMV_PEXEL_1 | 64 | 69 | PF00026 | 0.381 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P950 | Leptomonas seymouri | 25% | 87% |
A0A0N1ILX4 | Leptomonas seymouri | 60% | 100% |
A0A0S4JKE9 | Bodo saltans | 51% | 100% |
A0A1X0NTZ8 | Trypanosomatidae | 54% | 100% |
A0A1X0NZT5 | Trypanosomatidae | 25% | 100% |
A0A3Q8IAB6 | Leishmania donovani | 84% | 89% |
A0A3S5IRP3 | Trypanosoma rangeli | 54% | 100% |
A0A3S7X2J5 | Leishmania donovani | 26% | 90% |
A4HHF5 | Leishmania braziliensis | 26% | 96% |
A4HWL2 | Leishmania infantum | 85% | 89% |
A4I4K3 | Leishmania infantum | 26% | 90% |
C9ZL87 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 100% |
C9ZXS8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 53% | 100% |
E9AE02 | Leishmania major | 25% | 100% |
E9ALT0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 96% |
E9AQB9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 89% |
Q4QF55 | Leishmania major | 86% | 100% |
V5B4N1 | Trypanosoma cruzi | 54% | 100% |
V5D9T1 | Trypanosoma cruzi | 25% | 100% |