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 |
Related structures:
AlphaFold database: A4HMW4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 132 | 136 | PF00656 | 0.432 |
CLV_C14_Caspase3-7 | 368 | 372 | PF00656 | 0.473 |
CLV_NRD_NRD_1 | 216 | 218 | PF00675 | 0.591 |
CLV_NRD_NRD_1 | 318 | 320 | PF00675 | 0.277 |
CLV_NRD_NRD_1 | 354 | 356 | PF00675 | 0.401 |
CLV_PCSK_KEX2_1 | 215 | 217 | PF00082 | 0.487 |
CLV_PCSK_SKI1_1 | 355 | 359 | PF00082 | 0.505 |
CLV_PCSK_SKI1_1 | 6 | 10 | PF00082 | 0.704 |
CLV_PCSK_SKI1_1 | 93 | 97 | PF00082 | 0.442 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.631 |
DEG_SPOP_SBC_1 | 360 | 364 | PF00917 | 0.663 |
DOC_CYCLIN_RxL_1 | 352 | 363 | PF00134 | 0.397 |
DOC_CYCLIN_RxL_1 | 90 | 97 | PF00134 | 0.486 |
DOC_MAPK_gen_1 | 319 | 330 | PF00069 | 0.424 |
DOC_MAPK_gen_1 | 61 | 70 | PF00069 | 0.303 |
DOC_MAPK_MEF2A_6 | 167 | 174 | PF00069 | 0.484 |
DOC_PP2B_LxvP_1 | 357 | 360 | PF13499 | 0.613 |
DOC_USP7_MATH_1 | 115 | 119 | PF00917 | 0.547 |
DOC_USP7_MATH_1 | 168 | 172 | PF00917 | 0.705 |
DOC_USP7_MATH_1 | 179 | 183 | PF00917 | 0.596 |
DOC_USP7_MATH_1 | 189 | 193 | PF00917 | 0.684 |
DOC_USP7_MATH_1 | 198 | 202 | PF00917 | 0.554 |
DOC_USP7_MATH_1 | 360 | 364 | PF00917 | 0.689 |
DOC_WW_Pin1_4 | 194 | 199 | PF00397 | 0.802 |
DOC_WW_Pin1_4 | 201 | 206 | PF00397 | 0.654 |
DOC_WW_Pin1_4 | 209 | 214 | PF00397 | 0.557 |
DOC_WW_Pin1_4 | 79 | 84 | PF00397 | 0.421 |
LIG_14-3-3_CanoR_1 | 107 | 112 | PF00244 | 0.340 |
LIG_14-3-3_CanoR_1 | 146 | 156 | PF00244 | 0.483 |
LIG_14-3-3_CanoR_1 | 355 | 360 | PF00244 | 0.374 |
LIG_AP2alpha_1 | 133 | 137 | PF02296 | 0.417 |
LIG_BRCT_BRCA1_1 | 13 | 17 | PF00533 | 0.528 |
LIG_FHA_1 | 178 | 184 | PF00498 | 0.576 |
LIG_FHA_1 | 233 | 239 | PF00498 | 0.365 |
LIG_FHA_1 | 7 | 13 | PF00498 | 0.558 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.392 |
LIG_FHA_2 | 189 | 195 | PF00498 | 0.680 |
LIG_FHA_2 | 202 | 208 | PF00498 | 0.739 |
LIG_FHA_2 | 32 | 38 | PF00498 | 0.485 |
LIG_FHA_2 | 340 | 346 | PF00498 | 0.552 |
LIG_FHA_2 | 366 | 372 | PF00498 | 0.471 |
LIG_FHA_2 | 60 | 66 | PF00498 | 0.396 |
LIG_LIR_Apic_2 | 26 | 32 | PF02991 | 0.512 |
LIG_LIR_Gen_1 | 22 | 32 | PF02991 | 0.519 |
LIG_LIR_Gen_1 | 235 | 245 | PF02991 | 0.314 |
LIG_LIR_Nem_3 | 110 | 114 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 22 | 28 | PF02991 | 0.533 |
LIG_LIR_Nem_3 | 235 | 240 | PF02991 | 0.361 |
LIG_NRBOX | 273 | 279 | PF00104 | 0.380 |
LIG_NRBOX | 90 | 96 | PF00104 | 0.489 |
LIG_Pex14_2 | 133 | 137 | PF04695 | 0.373 |
LIG_Pex14_2 | 25 | 29 | PF04695 | 0.508 |
LIG_SH2_SRC | 311 | 314 | PF00017 | 0.372 |
LIG_SH2_STAP1 | 267 | 271 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 111 | 114 | PF00017 | 0.354 |
LIG_SH2_STAT5 | 311 | 314 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 42 | 45 | PF00017 | 0.463 |
LIG_SH3_3 | 192 | 198 | PF00018 | 0.553 |
LIG_SUMO_SIM_anti_2 | 325 | 332 | PF11976 | 0.455 |
LIG_TRAF2_1 | 372 | 375 | PF00917 | 0.753 |
LIG_TRFH_1 | 111 | 115 | PF08558 | 0.361 |
LIG_UBA3_1 | 277 | 281 | PF00899 | 0.352 |
LIG_UBA3_1 | 74 | 81 | PF00899 | 0.402 |
MOD_CDC14_SPxK_1 | 212 | 215 | PF00782 | 0.494 |
MOD_CDK_SPxK_1 | 209 | 215 | PF00069 | 0.504 |
MOD_CDK_SPxxK_3 | 209 | 216 | PF00069 | 0.503 |
MOD_CK1_1 | 118 | 124 | PF00069 | 0.581 |
MOD_CK1_1 | 201 | 207 | PF00069 | 0.689 |
MOD_CK1_1 | 211 | 217 | PF00069 | 0.661 |
MOD_CK1_1 | 363 | 369 | PF00069 | 0.653 |
MOD_CK1_1 | 63 | 69 | PF00069 | 0.346 |
MOD_CK2_1 | 118 | 124 | PF00069 | 0.660 |
MOD_CK2_1 | 156 | 162 | PF00069 | 0.491 |
MOD_CK2_1 | 188 | 194 | PF00069 | 0.760 |
MOD_CK2_1 | 222 | 228 | PF00069 | 0.558 |
MOD_CK2_1 | 31 | 37 | PF00069 | 0.500 |
MOD_CK2_1 | 319 | 325 | PF00069 | 0.273 |
MOD_CK2_1 | 339 | 345 | PF00069 | 0.556 |
MOD_CK2_1 | 47 | 53 | PF00069 | 0.341 |
MOD_CK2_1 | 63 | 69 | PF00069 | 0.285 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.517 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.455 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.754 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.717 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.614 |
MOD_GlcNHglycan | 303 | 307 | PF01048 | 0.398 |
MOD_GSK3_1 | 114 | 121 | PF00069 | 0.544 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.584 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.502 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.612 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.712 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.572 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.559 |
MOD_GSK3_1 | 363 | 370 | PF00069 | 0.654 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.339 |
MOD_N-GLC_1 | 115 | 120 | PF02516 | 0.549 |
MOD_N-GLC_1 | 19 | 24 | PF02516 | 0.590 |
MOD_N-GLC_1 | 79 | 84 | PF02516 | 0.446 |
MOD_N-GLC_2 | 147 | 149 | PF02516 | 0.484 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.535 |
MOD_NEK2_1 | 129 | 134 | PF00069 | 0.556 |
MOD_NEK2_1 | 232 | 237 | PF00069 | 0.342 |
MOD_NEK2_1 | 365 | 370 | PF00069 | 0.560 |
MOD_NEK2_1 | 47 | 52 | PF00069 | 0.495 |
MOD_PIKK_1 | 339 | 345 | PF00454 | 0.442 |
MOD_PK_1 | 217 | 223 | PF00069 | 0.477 |
MOD_PKA_1 | 319 | 325 | PF00069 | 0.273 |
MOD_PKA_1 | 355 | 361 | PF00069 | 0.383 |
MOD_PKA_2 | 60 | 66 | PF00069 | 0.331 |
MOD_PKB_1 | 215 | 223 | PF00069 | 0.464 |
MOD_Plk_1 | 115 | 121 | PF00069 | 0.615 |
MOD_Plk_1 | 232 | 238 | PF00069 | 0.324 |
MOD_Plk_1 | 269 | 275 | PF00069 | 0.430 |
MOD_Plk_1 | 47 | 53 | PF00069 | 0.473 |
MOD_Plk_4 | 107 | 113 | PF00069 | 0.388 |
MOD_Plk_4 | 217 | 223 | PF00069 | 0.597 |
MOD_Plk_4 | 47 | 53 | PF00069 | 0.588 |
MOD_Plk_4 | 63 | 69 | PF00069 | 0.254 |
MOD_ProDKin_1 | 194 | 200 | PF00069 | 0.800 |
MOD_ProDKin_1 | 201 | 207 | PF00069 | 0.655 |
MOD_ProDKin_1 | 209 | 215 | PF00069 | 0.554 |
MOD_ProDKin_1 | 79 | 85 | PF00069 | 0.423 |
MOD_SUMO_rev_2 | 201 | 211 | PF00179 | 0.651 |
MOD_SUMO_rev_2 | 349 | 358 | PF00179 | 0.449 |
MOD_SUMO_rev_2 | 77 | 83 | PF00179 | 0.425 |
TRG_DiLeu_BaEn_1 | 326 | 331 | PF01217 | 0.368 |
TRG_DiLeu_BaLyEn_6 | 153 | 158 | PF01217 | 0.446 |
TRG_DiLeu_BaLyEn_6 | 90 | 95 | PF01217 | 0.268 |
TRG_ENDOCYTIC_2 | 229 | 232 | PF00928 | 0.521 |
TRG_ER_diArg_1 | 215 | 217 | PF00400 | 0.487 |
TRG_Pf-PMV_PEXEL_1 | 73 | 77 | PF00026 | 0.386 |
TRG_Pf-PMV_PEXEL_1 | 93 | 97 | PF00026 | 0.388 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBE1 | Leptomonas seymouri | 66% | 100% |
A0A0S4JHH3 | Bodo saltans | 48% | 100% |
A0A1X0P5G2 | Trypanosomatidae | 55% | 100% |
A0A3S7X9G6 | Leishmania donovani | 81% | 100% |
A0A422P2T5 | Trypanosoma rangeli | 54% | 100% |
A4IBI5 | Leishmania infantum | 80% | 100% |
C9ZZ56 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 55% | 100% |
E9AFC1 | Leishmania major | 80% | 100% |
E9B6H6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |
V5BD06 | Trypanosoma cruzi | 55% | 100% |