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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: A4I4B0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 246 | 250 | PF00656 | 0.418 |
CLV_NRD_NRD_1 | 114 | 116 | PF00675 | 0.613 |
CLV_NRD_NRD_1 | 127 | 129 | PF00675 | 0.422 |
CLV_NRD_NRD_1 | 131 | 133 | PF00675 | 0.412 |
CLV_NRD_NRD_1 | 146 | 148 | PF00675 | 0.445 |
CLV_NRD_NRD_1 | 184 | 186 | PF00675 | 0.608 |
CLV_NRD_NRD_1 | 206 | 208 | PF00675 | 0.702 |
CLV_NRD_NRD_1 | 368 | 370 | PF00675 | 0.569 |
CLV_NRD_NRD_1 | 400 | 402 | PF00675 | 0.679 |
CLV_NRD_NRD_1 | 433 | 435 | PF00675 | 0.530 |
CLV_NRD_NRD_1 | 450 | 452 | PF00675 | 0.516 |
CLV_PCSK_FUR_1 | 125 | 129 | PF00082 | 0.468 |
CLV_PCSK_FUR_1 | 204 | 208 | PF00082 | 0.609 |
CLV_PCSK_FUR_1 | 448 | 452 | PF00082 | 0.452 |
CLV_PCSK_KEX2_1 | 116 | 118 | PF00082 | 0.493 |
CLV_PCSK_KEX2_1 | 125 | 127 | PF00082 | 0.454 |
CLV_PCSK_KEX2_1 | 130 | 132 | PF00082 | 0.385 |
CLV_PCSK_KEX2_1 | 145 | 147 | PF00082 | 0.483 |
CLV_PCSK_KEX2_1 | 184 | 186 | PF00082 | 0.608 |
CLV_PCSK_KEX2_1 | 206 | 208 | PF00082 | 0.702 |
CLV_PCSK_KEX2_1 | 368 | 370 | PF00082 | 0.569 |
CLV_PCSK_KEX2_1 | 400 | 402 | PF00082 | 0.677 |
CLV_PCSK_KEX2_1 | 433 | 435 | PF00082 | 0.534 |
CLV_PCSK_KEX2_1 | 450 | 452 | PF00082 | 0.516 |
CLV_PCSK_PC1ET2_1 | 116 | 118 | PF00082 | 0.362 |
CLV_PCSK_PC1ET2_1 | 145 | 147 | PF00082 | 0.588 |
CLV_PCSK_PC7_1 | 126 | 132 | PF00082 | 0.588 |
CLV_PCSK_PC7_1 | 446 | 452 | PF00082 | 0.446 |
CLV_PCSK_SKI1_1 | 142 | 146 | PF00082 | 0.418 |
CLV_PCSK_SKI1_1 | 226 | 230 | PF00082 | 0.748 |
CLV_PCSK_SKI1_1 | 328 | 332 | PF00082 | 0.613 |
DEG_SPOP_SBC_1 | 279 | 283 | PF00917 | 0.580 |
DEG_SPOP_SBC_1 | 294 | 298 | PF00917 | 0.493 |
DEG_SPOP_SBC_1 | 392 | 396 | PF00917 | 0.747 |
DEG_SPOP_SBC_1 | 455 | 459 | PF00917 | 0.603 |
DOC_CYCLIN_yCln2_LP_2 | 10 | 16 | PF00134 | 0.564 |
DOC_MAPK_DCC_7 | 185 | 195 | PF00069 | 0.581 |
DOC_MAPK_gen_1 | 113 | 121 | PF00069 | 0.472 |
DOC_MAPK_gen_1 | 446 | 455 | PF00069 | 0.545 |
DOC_MAPK_GRA24_9 | 181 | 195 | PF00069 | 0.573 |
DOC_MAPK_RevD_3 | 420 | 434 | PF00069 | 0.497 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.579 |
DOC_USP7_MATH_1 | 271 | 275 | PF00917 | 0.657 |
DOC_USP7_MATH_1 | 279 | 283 | PF00917 | 0.578 |
DOC_USP7_MATH_1 | 35 | 39 | PF00917 | 0.622 |
DOC_USP7_MATH_1 | 370 | 374 | PF00917 | 0.655 |
DOC_USP7_MATH_1 | 392 | 396 | PF00917 | 0.769 |
DOC_USP7_MATH_1 | 454 | 458 | PF00917 | 0.644 |
DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.574 |
DOC_USP7_UBL2_3 | 253 | 257 | PF12436 | 0.439 |
DOC_WW_Pin1_4 | 205 | 210 | PF00397 | 0.649 |
DOC_WW_Pin1_4 | 263 | 268 | PF00397 | 0.660 |
DOC_WW_Pin1_4 | 5 | 10 | PF00397 | 0.621 |
LIG_14-3-3_CanoR_1 | 328 | 333 | PF00244 | 0.583 |
LIG_14-3-3_CanoR_1 | 369 | 375 | PF00244 | 0.577 |
LIG_14-3-3_CanoR_1 | 390 | 398 | PF00244 | 0.636 |
LIG_BIR_III_4 | 249 | 253 | PF00653 | 0.490 |
LIG_DLG_GKlike_1 | 90 | 98 | PF00625 | 0.439 |
LIG_eIF4E_1 | 171 | 177 | PF01652 | 0.562 |
LIG_FHA_1 | 167 | 173 | PF00498 | 0.597 |
LIG_FHA_1 | 457 | 463 | PF00498 | 0.651 |
LIG_FHA_2 | 233 | 239 | PF00498 | 0.602 |
LIG_FHA_2 | 244 | 250 | PF00498 | 0.405 |
LIG_FHA_2 | 279 | 285 | PF00498 | 0.755 |
LIG_FHA_2 | 309 | 315 | PF00498 | 0.552 |
LIG_FHA_2 | 329 | 335 | PF00498 | 0.559 |
LIG_FHA_2 | 439 | 445 | PF00498 | 0.562 |
LIG_Integrin_RGD_1 | 469 | 471 | PF01839 | 0.594 |
LIG_LIR_Apic_2 | 323 | 329 | PF02991 | 0.642 |
LIG_LIR_Gen_1 | 342 | 350 | PF02991 | 0.428 |
LIG_LIR_Gen_1 | 418 | 426 | PF02991 | 0.548 |
LIG_LIR_Gen_1 | 51 | 61 | PF02991 | 0.583 |
LIG_LIR_Gen_1 | 62 | 71 | PF02991 | 0.516 |
LIG_LIR_Nem_3 | 342 | 348 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 418 | 422 | PF02991 | 0.547 |
LIG_LIR_Nem_3 | 51 | 57 | PF02991 | 0.597 |
LIG_LIR_Nem_3 | 62 | 67 | PF02991 | 0.523 |
LIG_MYND_1 | 12 | 16 | PF01753 | 0.595 |
LIG_SH2_CRK | 345 | 349 | PF00017 | 0.430 |
LIG_SH2_SRC | 171 | 174 | PF00017 | 0.565 |
LIG_SH2_STAP1 | 50 | 54 | PF00017 | 0.600 |
LIG_SH2_STAP1 | 94 | 98 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 171 | 174 | PF00017 | 0.604 |
LIG_SH2_STAT5 | 63 | 66 | PF00017 | 0.543 |
LIG_SH3_1 | 206 | 212 | PF00018 | 0.604 |
LIG_SH3_3 | 191 | 197 | PF00018 | 0.604 |
LIG_SH3_3 | 206 | 212 | PF00018 | 0.540 |
LIG_SH3_3 | 6 | 12 | PF00018 | 0.573 |
LIG_TRAF2_1 | 236 | 239 | PF00917 | 0.473 |
LIG_TRAF2_1 | 39 | 42 | PF00917 | 0.590 |
LIG_TRAF2_1 | 70 | 73 | PF00917 | 0.403 |
LIG_UBA3_1 | 67 | 74 | PF00899 | 0.465 |
MOD_CK1_1 | 232 | 238 | PF00069 | 0.651 |
MOD_CK1_1 | 272 | 278 | PF00069 | 0.749 |
MOD_CK1_1 | 36 | 42 | PF00069 | 0.570 |
MOD_CK1_1 | 394 | 400 | PF00069 | 0.651 |
MOD_CK1_1 | 457 | 463 | PF00069 | 0.642 |
MOD_CK1_1 | 477 | 483 | PF00069 | 0.401 |
MOD_CK1_1 | 5 | 11 | PF00069 | 0.689 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.544 |
MOD_CK1_1 | 79 | 85 | PF00069 | 0.625 |
MOD_CK2_1 | 196 | 202 | PF00069 | 0.656 |
MOD_CK2_1 | 232 | 238 | PF00069 | 0.576 |
MOD_CK2_1 | 278 | 284 | PF00069 | 0.668 |
MOD_CK2_1 | 328 | 334 | PF00069 | 0.532 |
MOD_CK2_1 | 35 | 41 | PF00069 | 0.588 |
MOD_CK2_1 | 438 | 444 | PF00069 | 0.565 |
MOD_CK2_1 | 67 | 73 | PF00069 | 0.527 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.700 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.677 |
MOD_GlcNHglycan | 220 | 223 | PF01048 | 0.676 |
MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.540 |
MOD_GlcNHglycan | 297 | 300 | PF01048 | 0.737 |
MOD_GlcNHglycan | 35 | 38 | PF01048 | 0.615 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.717 |
MOD_GlcNHglycan | 476 | 479 | PF01048 | 0.543 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.518 |
MOD_GlcNHglycan | 82 | 85 | PF01048 | 0.528 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.663 |
MOD_GSK3_1 | 229 | 236 | PF00069 | 0.646 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.651 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.646 |
MOD_GSK3_1 | 388 | 395 | PF00069 | 0.671 |
MOD_GSK3_1 | 454 | 461 | PF00069 | 0.653 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.572 |
MOD_GSK3_1 | 86 | 93 | PF00069 | 0.531 |
MOD_N-GLC_1 | 229 | 234 | PF02516 | 0.521 |
MOD_PIKK_1 | 166 | 172 | PF00454 | 0.681 |
MOD_PIKK_1 | 243 | 249 | PF00454 | 0.502 |
MOD_PIKK_1 | 265 | 271 | PF00454 | 0.625 |
MOD_PK_1 | 410 | 416 | PF00069 | 0.571 |
MOD_PKA_1 | 126 | 132 | PF00069 | 0.459 |
MOD_PKA_2 | 126 | 132 | PF00069 | 0.459 |
MOD_PKA_2 | 294 | 300 | PF00069 | 0.591 |
MOD_PKA_2 | 474 | 480 | PF00069 | 0.581 |
MOD_Plk_1 | 40 | 46 | PF00069 | 0.647 |
MOD_Plk_1 | 438 | 444 | PF00069 | 0.581 |
MOD_Plk_1 | 59 | 65 | PF00069 | 0.528 |
MOD_Plk_2-3 | 438 | 444 | PF00069 | 0.581 |
MOD_Plk_4 | 220 | 226 | PF00069 | 0.638 |
MOD_ProDKin_1 | 205 | 211 | PF00069 | 0.649 |
MOD_ProDKin_1 | 263 | 269 | PF00069 | 0.661 |
MOD_ProDKin_1 | 5 | 11 | PF00069 | 0.624 |
TRG_DiLeu_BaEn_4 | 72 | 78 | PF01217 | 0.422 |
TRG_DiLeu_BaLyEn_6 | 6 | 11 | PF01217 | 0.574 |
TRG_ENDOCYTIC_2 | 345 | 348 | PF00928 | 0.442 |
TRG_ER_diArg_1 | 112 | 115 | PF00400 | 0.535 |
TRG_ER_diArg_1 | 125 | 128 | PF00400 | 0.426 |
TRG_ER_diArg_1 | 130 | 132 | PF00400 | 0.388 |
TRG_ER_diArg_1 | 146 | 148 | PF00400 | 0.410 |
TRG_ER_diArg_1 | 184 | 187 | PF00400 | 0.581 |
TRG_ER_diArg_1 | 204 | 207 | PF00400 | 0.762 |
TRG_ER_diArg_1 | 367 | 369 | PF00400 | 0.563 |
TRG_ER_diArg_1 | 433 | 435 | PF00400 | 0.561 |
TRG_ER_diArg_1 | 448 | 451 | PF00400 | 0.521 |
TRG_ER_diArg_1 | 463 | 466 | PF00400 | 0.587 |
TRG_NLS_Bipartite_1 | 127 | 149 | PF00514 | 0.492 |
TRG_NLS_MonoExtN_4 | 113 | 119 | PF00514 | 0.364 |
TRG_NLS_MonoExtN_4 | 142 | 149 | PF00514 | 0.424 |
TRG_Pf-PMV_PEXEL_1 | 102 | 106 | PF00026 | 0.499 |
TRG_Pf-PMV_PEXEL_1 | 107 | 111 | PF00026 | 0.468 |
TRG_Pf-PMV_PEXEL_1 | 433 | 437 | PF00026 | 0.522 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCW8 | Leptomonas seymouri | 39% | 97% |
A0A1X0NZK9 | Trypanosomatidae | 24% | 95% |
A0A3Q8IF08 | Leishmania donovani | 99% | 100% |
A4HH66 | Leishmania braziliensis | 64% | 99% |
E9ADR0 | Leishmania major | 91% | 100% |
E9AM20 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |