Uncharacterized Protein, Uncharacterized
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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: E9AGV8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 386 | 390 | PF00656 | 0.495 |
CLV_C14_Caspase3-7 | 406 | 410 | PF00656 | 0.487 |
CLV_NRD_NRD_1 | 133 | 135 | PF00675 | 0.563 |
CLV_NRD_NRD_1 | 200 | 202 | PF00675 | 0.647 |
CLV_NRD_NRD_1 | 251 | 253 | PF00675 | 0.503 |
CLV_NRD_NRD_1 | 275 | 277 | PF00675 | 0.585 |
CLV_NRD_NRD_1 | 340 | 342 | PF00675 | 0.600 |
CLV_NRD_NRD_1 | 344 | 346 | PF00675 | 0.558 |
CLV_NRD_NRD_1 | 368 | 370 | PF00675 | 0.512 |
CLV_PCSK_KEX2_1 | 133 | 135 | PF00082 | 0.563 |
CLV_PCSK_KEX2_1 | 199 | 201 | PF00082 | 0.770 |
CLV_PCSK_KEX2_1 | 251 | 253 | PF00082 | 0.503 |
CLV_PCSK_KEX2_1 | 275 | 277 | PF00082 | 0.583 |
CLV_PCSK_KEX2_1 | 340 | 342 | PF00082 | 0.587 |
CLV_PCSK_SKI1_1 | 11 | 15 | PF00082 | 0.513 |
CLV_PCSK_SKI1_1 | 306 | 310 | PF00082 | 0.603 |
DEG_SCF_FBW7_1 | 100 | 105 | PF00400 | 0.583 |
DEG_SPOP_SBC_1 | 102 | 106 | PF00917 | 0.545 |
DEG_SPOP_SBC_1 | 318 | 322 | PF00917 | 0.633 |
DOC_ANK_TNKS_1 | 199 | 206 | PF00023 | 0.532 |
DOC_MAPK_gen_1 | 251 | 257 | PF00069 | 0.435 |
DOC_MAPK_gen_1 | 275 | 282 | PF00069 | 0.533 |
DOC_MAPK_MEF2A_6 | 110 | 118 | PF00069 | 0.435 |
DOC_MAPK_MEF2A_6 | 275 | 284 | PF00069 | 0.528 |
DOC_PP1_RVXF_1 | 9 | 16 | PF00149 | 0.439 |
DOC_PP2B_LxvP_1 | 36 | 39 | PF13499 | 0.547 |
DOC_USP7_MATH_1 | 103 | 107 | PF00917 | 0.569 |
DOC_USP7_MATH_1 | 167 | 171 | PF00917 | 0.741 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.558 |
DOC_USP7_MATH_1 | 317 | 321 | PF00917 | 0.715 |
DOC_USP7_MATH_1 | 325 | 329 | PF00917 | 0.688 |
DOC_WW_Pin1_4 | 98 | 103 | PF00397 | 0.606 |
LIG_14-3-3_CanoR_1 | 11 | 16 | PF00244 | 0.589 |
LIG_14-3-3_CanoR_1 | 110 | 114 | PF00244 | 0.474 |
LIG_14-3-3_CanoR_1 | 275 | 282 | PF00244 | 0.533 |
LIG_14-3-3_CanoR_1 | 369 | 373 | PF00244 | 0.521 |
LIG_14-3-3_CanoR_1 | 4 | 8 | PF00244 | 0.569 |
LIG_Actin_WH2_2 | 72 | 88 | PF00022 | 0.503 |
LIG_BRCT_BRCA1_1 | 28 | 32 | PF00533 | 0.393 |
LIG_FHA_1 | 103 | 109 | PF00498 | 0.635 |
LIG_FHA_1 | 110 | 116 | PF00498 | 0.425 |
LIG_FHA_1 | 17 | 23 | PF00498 | 0.398 |
LIG_FHA_1 | 217 | 223 | PF00498 | 0.581 |
LIG_FHA_1 | 295 | 301 | PF00498 | 0.496 |
LIG_FHA_1 | 355 | 361 | PF00498 | 0.465 |
LIG_FHA_1 | 80 | 86 | PF00498 | 0.403 |
LIG_FHA_2 | 175 | 181 | PF00498 | 0.704 |
LIG_FHA_2 | 231 | 237 | PF00498 | 0.439 |
LIG_FHA_2 | 442 | 448 | PF00498 | 0.597 |
LIG_LIR_Gen_1 | 112 | 120 | PF02991 | 0.385 |
LIG_LIR_Gen_1 | 29 | 39 | PF02991 | 0.421 |
LIG_LIR_Gen_1 | 350 | 360 | PF02991 | 0.513 |
LIG_LIR_Gen_1 | 430 | 439 | PF02991 | 0.546 |
LIG_LIR_Gen_1 | 59 | 66 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 112 | 116 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 29 | 35 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 350 | 355 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 430 | 434 | PF02991 | 0.571 |
LIG_LIR_Nem_3 | 59 | 64 | PF02991 | 0.497 |
LIG_SH2_PTP2 | 113 | 116 | PF00017 | 0.422 |
LIG_SH2_SRC | 148 | 151 | PF00017 | 0.388 |
LIG_SH2_SRC | 387 | 390 | PF00017 | 0.500 |
LIG_SH2_STAP1 | 356 | 360 | PF00017 | 0.496 |
LIG_SH2_STAP1 | 421 | 425 | PF00017 | 0.604 |
LIG_SH2_STAT5 | 113 | 116 | PF00017 | 0.542 |
LIG_SH2_STAT5 | 148 | 151 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 356 | 359 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 387 | 390 | PF00017 | 0.500 |
LIG_SH3_3 | 10 | 16 | PF00018 | 0.494 |
LIG_SH3_3 | 257 | 263 | PF00018 | 0.636 |
LIG_SH3_3 | 411 | 417 | PF00018 | 0.613 |
LIG_SUMO_SIM_anti_2 | 112 | 119 | PF11976 | 0.427 |
LIG_SUMO_SIM_anti_2 | 211 | 216 | PF11976 | 0.362 |
LIG_SUMO_SIM_par_1 | 112 | 119 | PF11976 | 0.383 |
LIG_SUMO_SIM_par_1 | 280 | 285 | PF11976 | 0.446 |
LIG_UBA3_1 | 299 | 306 | PF00899 | 0.475 |
LIG_WRC_WIRS_1 | 363 | 368 | PF05994 | 0.568 |
LIG_WW_3 | 64 | 68 | PF00397 | 0.433 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.659 |
MOD_CK1_1 | 358 | 364 | PF00069 | 0.473 |
MOD_CK1_1 | 403 | 409 | PF00069 | 0.564 |
MOD_CK2_1 | 230 | 236 | PF00069 | 0.456 |
MOD_CK2_1 | 255 | 261 | PF00069 | 0.495 |
MOD_CK2_1 | 362 | 368 | PF00069 | 0.492 |
MOD_CK2_1 | 441 | 447 | PF00069 | 0.591 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.602 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.547 |
MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.377 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.758 |
MOD_GlcNHglycan | 173 | 176 | PF01048 | 0.699 |
MOD_GlcNHglycan | 222 | 225 | PF01048 | 0.638 |
MOD_GlcNHglycan | 241 | 244 | PF01048 | 0.340 |
MOD_GlcNHglycan | 247 | 250 | PF01048 | 0.432 |
MOD_GlcNHglycan | 270 | 273 | PF01048 | 0.611 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.687 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.598 |
MOD_GlcNHglycan | 393 | 396 | PF01048 | 0.732 |
MOD_GlcNHglycan | 403 | 406 | PF01048 | 0.595 |
MOD_GlcNHglycan | 435 | 438 | PF01048 | 0.540 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.587 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.492 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.762 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.591 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.600 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.612 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.500 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.521 |
MOD_GSK3_1 | 373 | 380 | PF00069 | 0.461 |
MOD_GSK3_1 | 387 | 394 | PF00069 | 0.496 |
MOD_GSK3_1 | 399 | 406 | PF00069 | 0.585 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.666 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.654 |
MOD_N-GLC_1 | 181 | 186 | PF02516 | 0.640 |
MOD_N-GLC_1 | 216 | 221 | PF02516 | 0.510 |
MOD_N-GLC_1 | 225 | 230 | PF02516 | 0.548 |
MOD_N-GLC_2 | 268 | 270 | PF02516 | 0.583 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.548 |
MOD_NEK2_1 | 286 | 291 | PF00069 | 0.412 |
MOD_NEK2_1 | 3 | 8 | PF00069 | 0.597 |
MOD_NEK2_1 | 355 | 360 | PF00069 | 0.463 |
MOD_NEK2_2 | 16 | 21 | PF00069 | 0.401 |
MOD_NEK2_2 | 319 | 324 | PF00069 | 0.613 |
MOD_NEK2_2 | 56 | 61 | PF00069 | 0.532 |
MOD_PIKK_1 | 294 | 300 | PF00454 | 0.416 |
MOD_PIKK_1 | 340 | 346 | PF00454 | 0.576 |
MOD_PIKK_1 | 65 | 71 | PF00454 | 0.424 |
MOD_PIKK_1 | 77 | 83 | PF00454 | 0.483 |
MOD_PKA_1 | 340 | 346 | PF00069 | 0.580 |
MOD_PKA_2 | 109 | 115 | PF00069 | 0.477 |
MOD_PKA_2 | 274 | 280 | PF00069 | 0.556 |
MOD_PKA_2 | 3 | 9 | PF00069 | 0.557 |
MOD_PKA_2 | 340 | 346 | PF00069 | 0.580 |
MOD_PKA_2 | 368 | 374 | PF00069 | 0.485 |
MOD_Plk_1 | 26 | 32 | PF00069 | 0.388 |
MOD_Plk_1 | 361 | 367 | PF00069 | 0.466 |
MOD_Plk_2-3 | 362 | 368 | PF00069 | 0.492 |
MOD_Plk_4 | 109 | 115 | PF00069 | 0.453 |
MOD_Plk_4 | 208 | 214 | PF00069 | 0.404 |
MOD_Plk_4 | 319 | 325 | PF00069 | 0.637 |
MOD_Plk_4 | 355 | 361 | PF00069 | 0.465 |
MOD_Plk_4 | 56 | 62 | PF00069 | 0.537 |
MOD_Plk_4 | 79 | 85 | PF00069 | 0.397 |
MOD_ProDKin_1 | 98 | 104 | PF00069 | 0.600 |
MOD_SUMO_rev_2 | 362 | 372 | PF00179 | 0.493 |
TRG_ENDOCYTIC_2 | 113 | 116 | PF00928 | 0.370 |
TRG_ENDOCYTIC_2 | 356 | 359 | PF00928 | 0.499 |
TRG_ER_diArg_1 | 199 | 201 | PF00400 | 0.683 |
TRG_ER_diArg_1 | 339 | 341 | PF00400 | 0.625 |
TRG_Pf-PMV_PEXEL_1 | 252 | 256 | PF00026 | 0.461 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1ILY1 | Leptomonas seymouri | 48% | 100% |
A0A3S7WWI8 | Leishmania donovani | 100% | 100% |
A4HK96 | Leishmania braziliensis | 69% | 99% |
E9AV74 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 98% |
Q4QCA7 | Leishmania major | 91% | 100% |