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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 5 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
Related structures:
AlphaFold database: A4H4Z9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 107 | 111 | PF00656 | 0.693 |
CLV_C14_Caspase3-7 | 179 | 183 | PF00656 | 0.653 |
CLV_NRD_NRD_1 | 100 | 102 | PF00675 | 0.386 |
CLV_NRD_NRD_1 | 103 | 105 | PF00675 | 0.404 |
CLV_NRD_NRD_1 | 147 | 149 | PF00675 | 0.450 |
CLV_NRD_NRD_1 | 211 | 213 | PF00675 | 0.414 |
CLV_NRD_NRD_1 | 299 | 301 | PF00675 | 0.440 |
CLV_PCSK_KEX2_1 | 147 | 149 | PF00082 | 0.429 |
CLV_PCSK_KEX2_1 | 211 | 213 | PF00082 | 0.406 |
CLV_PCSK_KEX2_1 | 224 | 226 | PF00082 | 0.350 |
CLV_PCSK_KEX2_1 | 299 | 301 | PF00082 | 0.417 |
CLV_PCSK_KEX2_1 | 311 | 313 | PF00082 | 0.369 |
CLV_PCSK_KEX2_1 | 99 | 101 | PF00082 | 0.389 |
CLV_PCSK_PC1ET2_1 | 211 | 213 | PF00082 | 0.435 |
CLV_PCSK_PC1ET2_1 | 224 | 226 | PF00082 | 0.438 |
CLV_PCSK_PC1ET2_1 | 311 | 313 | PF00082 | 0.342 |
CLV_PCSK_PC7_1 | 95 | 101 | PF00082 | 0.389 |
CLV_PCSK_SKI1_1 | 113 | 117 | PF00082 | 0.511 |
CLV_PCSK_SKI1_1 | 299 | 303 | PF00082 | 0.412 |
CLV_PCSK_SKI1_1 | 59 | 63 | PF00082 | 0.585 |
CLV_PCSK_SKI1_1 | 88 | 92 | PF00082 | 0.382 |
DEG_SPOP_SBC_1 | 32 | 36 | PF00917 | 0.477 |
DEG_SPOP_SBC_1 | 381 | 385 | PF00917 | 0.696 |
DOC_MAPK_DCC_7 | 59 | 69 | PF00069 | 0.424 |
DOC_MAPK_FxFP_2 | 205 | 208 | PF00069 | 0.653 |
DOC_MAPK_gen_1 | 160 | 170 | PF00069 | 0.576 |
DOC_MAPK_gen_1 | 311 | 319 | PF00069 | 0.694 |
DOC_MAPK_MEF2A_6 | 154 | 161 | PF00069 | 0.599 |
DOC_MAPK_RevD_3 | 85 | 100 | PF00069 | 0.556 |
DOC_PP1_RVXF_1 | 57 | 63 | PF00149 | 0.419 |
DOC_PP2B_LxvP_1 | 67 | 70 | PF13499 | 0.356 |
DOC_PP4_FxxP_1 | 205 | 208 | PF00568 | 0.562 |
DOC_USP7_MATH_1 | 229 | 233 | PF00917 | 0.684 |
DOC_USP7_MATH_1 | 26 | 30 | PF00917 | 0.567 |
DOC_USP7_MATH_1 | 32 | 36 | PF00917 | 0.535 |
DOC_USP7_MATH_1 | 320 | 324 | PF00917 | 0.719 |
DOC_USP7_MATH_1 | 334 | 338 | PF00917 | 0.732 |
DOC_USP7_MATH_1 | 370 | 374 | PF00917 | 0.767 |
DOC_WW_Pin1_4 | 24 | 29 | PF00397 | 0.414 |
DOC_WW_Pin1_4 | 246 | 251 | PF00397 | 0.764 |
DOC_WW_Pin1_4 | 274 | 279 | PF00397 | 0.775 |
LIG_14-3-3_CanoR_1 | 113 | 119 | PF00244 | 0.655 |
LIG_14-3-3_CanoR_1 | 154 | 158 | PF00244 | 0.583 |
LIG_14-3-3_CanoR_1 | 173 | 181 | PF00244 | 0.533 |
LIG_14-3-3_CanoR_1 | 188 | 196 | PF00244 | 0.479 |
LIG_14-3-3_CanoR_1 | 233 | 239 | PF00244 | 0.716 |
LIG_14-3-3_CanoR_1 | 299 | 305 | PF00244 | 0.699 |
LIG_14-3-3_CanoR_1 | 372 | 378 | PF00244 | 0.725 |
LIG_14-3-3_CanoR_1 | 380 | 387 | PF00244 | 0.654 |
LIG_14-3-3_CanoR_1 | 47 | 54 | PF00244 | 0.417 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.372 |
LIG_BRCT_BRCA1_1 | 294 | 298 | PF00533 | 0.718 |
LIG_BRCT_BRCA1_1 | 5 | 9 | PF00533 | 0.376 |
LIG_CaM_NSCaTE_8 | 44 | 51 | PF13499 | 0.429 |
LIG_CSL_BTD_1 | 67 | 70 | PF09270 | 0.328 |
LIG_FHA_1 | 115 | 121 | PF00498 | 0.666 |
LIG_FHA_1 | 199 | 205 | PF00498 | 0.580 |
LIG_FHA_1 | 376 | 382 | PF00498 | 0.692 |
LIG_FHA_1 | 53 | 59 | PF00498 | 0.469 |
LIG_FHA_1 | 78 | 84 | PF00498 | 0.350 |
LIG_FHA_2 | 177 | 183 | PF00498 | 0.675 |
LIG_FHA_2 | 51 | 57 | PF00498 | 0.351 |
LIG_LIR_Apic_2 | 203 | 209 | PF02991 | 0.567 |
LIG_LIR_Gen_1 | 103 | 112 | PF02991 | 0.637 |
LIG_LIR_Gen_1 | 42 | 51 | PF02991 | 0.434 |
LIG_LIR_Gen_1 | 80 | 90 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 103 | 109 | PF02991 | 0.603 |
LIG_LIR_Nem_3 | 182 | 187 | PF02991 | 0.554 |
LIG_LIR_Nem_3 | 376 | 382 | PF02991 | 0.694 |
LIG_LIR_Nem_3 | 42 | 48 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 80 | 85 | PF02991 | 0.440 |
LIG_Pex14_1 | 45 | 49 | PF04695 | 0.426 |
LIG_Pex14_2 | 298 | 302 | PF04695 | 0.611 |
LIG_Pex14_2 | 90 | 94 | PF04695 | 0.551 |
LIG_SH2_CRK | 379 | 383 | PF00017 | 0.693 |
LIG_SH2_STAP1 | 41 | 45 | PF00017 | 0.309 |
LIG_SH2_STAT5 | 304 | 307 | PF00017 | 0.603 |
LIG_SH2_STAT5 | 82 | 85 | PF00017 | 0.331 |
LIG_SH3_3 | 284 | 290 | PF00018 | 0.597 |
LIG_WRC_WIRS_1 | 82 | 87 | PF05994 | 0.370 |
MOD_CDC14_SPxK_1 | 249 | 252 | PF00782 | 0.797 |
MOD_CDK_SPxK_1 | 246 | 252 | PF00069 | 0.794 |
MOD_CK1_1 | 246 | 252 | PF00069 | 0.750 |
MOD_CK1_1 | 261 | 267 | PF00069 | 0.681 |
MOD_CK1_1 | 269 | 275 | PF00069 | 0.651 |
MOD_CK1_1 | 27 | 33 | PF00069 | 0.523 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.493 |
MOD_CK1_1 | 327 | 333 | PF00069 | 0.736 |
MOD_CK1_1 | 34 | 40 | PF00069 | 0.457 |
MOD_CK1_1 | 373 | 379 | PF00069 | 0.745 |
MOD_CK1_1 | 383 | 389 | PF00069 | 0.650 |
MOD_CK1_1 | 50 | 56 | PF00069 | 0.292 |
MOD_CK2_1 | 261 | 267 | PF00069 | 0.808 |
MOD_CK2_1 | 319 | 325 | PF00069 | 0.720 |
MOD_CK2_1 | 50 | 56 | PF00069 | 0.395 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.726 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.387 |
MOD_GlcNHglycan | 267 | 271 | PF01048 | 0.557 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.741 |
MOD_GlcNHglycan | 325 | 329 | PF01048 | 0.535 |
MOD_GlcNHglycan | 332 | 335 | PF01048 | 0.554 |
MOD_GlcNHglycan | 336 | 339 | PF01048 | 0.530 |
MOD_GlcNHglycan | 343 | 346 | PF01048 | 0.486 |
MOD_GlcNHglycan | 349 | 352 | PF01048 | 0.428 |
MOD_GlcNHglycan | 357 | 360 | PF01048 | 0.418 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.639 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.512 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.562 |
MOD_GSK3_1 | 242 | 249 | PF00069 | 0.714 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.680 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.460 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.694 |
MOD_GSK3_1 | 330 | 337 | PF00069 | 0.711 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.700 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.757 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.471 |
MOD_N-GLC_1 | 234 | 239 | PF02516 | 0.494 |
MOD_N-GLC_1 | 243 | 248 | PF02516 | 0.497 |
MOD_N-GLC_1 | 274 | 279 | PF02516 | 0.568 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.372 |
MOD_NEK2_1 | 153 | 158 | PF00069 | 0.563 |
MOD_NEK2_1 | 176 | 181 | PF00069 | 0.616 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.512 |
MOD_NEK2_1 | 243 | 248 | PF00069 | 0.749 |
MOD_NEK2_1 | 294 | 299 | PF00069 | 0.671 |
MOD_NEK2_1 | 319 | 324 | PF00069 | 0.722 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.364 |
MOD_NEK2_2 | 81 | 86 | PF00069 | 0.327 |
MOD_PIKK_1 | 198 | 204 | PF00454 | 0.572 |
MOD_PIKK_1 | 39 | 45 | PF00454 | 0.344 |
MOD_PKA_2 | 153 | 159 | PF00069 | 0.573 |
MOD_PKA_2 | 187 | 193 | PF00069 | 0.560 |
MOD_PKA_2 | 262 | 268 | PF00069 | 0.749 |
MOD_PKA_2 | 320 | 326 | PF00069 | 0.692 |
MOD_PKA_2 | 371 | 377 | PF00069 | 0.769 |
MOD_Plk_1 | 140 | 146 | PF00069 | 0.647 |
MOD_Plk_1 | 234 | 240 | PF00069 | 0.714 |
MOD_Plk_1 | 243 | 249 | PF00069 | 0.715 |
MOD_Plk_4 | 77 | 83 | PF00069 | 0.396 |
MOD_ProDKin_1 | 24 | 30 | PF00069 | 0.414 |
MOD_ProDKin_1 | 246 | 252 | PF00069 | 0.767 |
MOD_ProDKin_1 | 274 | 280 | PF00069 | 0.777 |
MOD_SUMO_rev_2 | 303 | 313 | PF00179 | 0.633 |
TRG_ENDOCYTIC_2 | 106 | 109 | PF00928 | 0.621 |
TRG_ENDOCYTIC_2 | 379 | 382 | PF00928 | 0.694 |
TRG_ENDOCYTIC_2 | 82 | 85 | PF00928 | 0.373 |
TRG_ER_diArg_1 | 298 | 300 | PF00400 | 0.640 |
TRG_ER_diArg_1 | 85 | 88 | PF00400 | 0.406 |
TRG_ER_diArg_1 | 99 | 101 | PF00400 | 0.559 |
TRG_NES_CRM1_1 | 165 | 178 | PF08389 | 0.553 |
TRG_NLS_Bipartite_1 | 211 | 227 | PF00514 | 0.637 |
TRG_NLS_MonoExtC_3 | 222 | 227 | PF00514 | 0.668 |
TRG_Pf-PMV_PEXEL_1 | 173 | 178 | PF00026 | 0.443 |
TRG_Pf-PMV_PEXEL_1 | 215 | 219 | PF00026 | 0.489 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HSU4 | Leptomonas seymouri | 70% | 100% |
A0A0S4IXL3 | Bodo saltans | 32% | 100% |
A0A1X0NPE0 | Trypanosomatidae | 38% | 100% |
A0A3R7NBC4 | Trypanosoma rangeli | 46% | 100% |
A0A3S7WPV5 | Leishmania donovani | 86% | 99% |
A4HT79 | Leishmania infantum | 88% | 100% |
C9ZUQ2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
E9AL61 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
Q4QIP3 | Leishmania major | 87% | 100% |
V5B859 | Trypanosoma cruzi | 44% | 100% |