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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: A4I9G6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 250 | 254 | PF00656 | 0.556 |
CLV_C14_Caspase3-7 | 268 | 272 | PF00656 | 0.457 |
CLV_C14_Caspase3-7 | 80 | 84 | PF00656 | 0.484 |
CLV_NRD_NRD_1 | 111 | 113 | PF00675 | 0.607 |
CLV_NRD_NRD_1 | 13 | 15 | PF00675 | 0.549 |
CLV_NRD_NRD_1 | 154 | 156 | PF00675 | 0.530 |
CLV_NRD_NRD_1 | 206 | 208 | PF00675 | 0.560 |
CLV_NRD_NRD_1 | 290 | 292 | PF00675 | 0.725 |
CLV_NRD_NRD_1 | 318 | 320 | PF00675 | 0.677 |
CLV_NRD_NRD_1 | 341 | 343 | PF00675 | 0.700 |
CLV_NRD_NRD_1 | 37 | 39 | PF00675 | 0.585 |
CLV_NRD_NRD_1 | 392 | 394 | PF00675 | 0.638 |
CLV_NRD_NRD_1 | 68 | 70 | PF00675 | 0.435 |
CLV_NRD_NRD_1 | 89 | 91 | PF00675 | 0.502 |
CLV_PCSK_FUR_1 | 11 | 15 | PF00082 | 0.551 |
CLV_PCSK_KEX2_1 | 13 | 15 | PF00082 | 0.549 |
CLV_PCSK_KEX2_1 | 142 | 144 | PF00082 | 0.555 |
CLV_PCSK_KEX2_1 | 154 | 156 | PF00082 | 0.425 |
CLV_PCSK_KEX2_1 | 205 | 207 | PF00082 | 0.525 |
CLV_PCSK_KEX2_1 | 221 | 223 | PF00082 | 0.374 |
CLV_PCSK_KEX2_1 | 340 | 342 | PF00082 | 0.701 |
CLV_PCSK_KEX2_1 | 37 | 39 | PF00082 | 0.478 |
CLV_PCSK_KEX2_1 | 392 | 394 | PF00082 | 0.638 |
CLV_PCSK_KEX2_1 | 68 | 70 | PF00082 | 0.435 |
CLV_PCSK_PC1ET2_1 | 142 | 144 | PF00082 | 0.531 |
CLV_PCSK_PC1ET2_1 | 221 | 223 | PF00082 | 0.513 |
CLV_PCSK_SKI1_1 | 118 | 122 | PF00082 | 0.648 |
CLV_PCSK_SKI1_1 | 142 | 146 | PF00082 | 0.580 |
CLV_PCSK_SKI1_1 | 165 | 169 | PF00082 | 0.531 |
CLV_PCSK_SKI1_1 | 3 | 7 | PF00082 | 0.531 |
CLV_PCSK_SKI1_1 | 68 | 72 | PF00082 | 0.482 |
DEG_APCC_DBOX_1 | 93 | 101 | PF00400 | 0.453 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.627 |
DEG_SPOP_SBC_1 | 286 | 290 | PF00917 | 0.734 |
DEG_SPOP_SBC_1 | 422 | 426 | PF00917 | 0.539 |
DOC_CKS1_1 | 314 | 319 | PF01111 | 0.629 |
DOC_CKS1_1 | 336 | 341 | PF01111 | 0.695 |
DOC_MAPK_gen_1 | 211 | 219 | PF00069 | 0.488 |
DOC_MAPK_MEF2A_6 | 211 | 219 | PF00069 | 0.488 |
DOC_USP7_MATH_1 | 233 | 237 | PF00917 | 0.501 |
DOC_USP7_MATH_1 | 285 | 289 | PF00917 | 0.736 |
DOC_USP7_MATH_1 | 370 | 374 | PF00917 | 0.704 |
DOC_USP7_MATH_1 | 386 | 390 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 430 | 434 | PF00917 | 0.690 |
DOC_USP7_MATH_1 | 436 | 440 | PF00917 | 0.611 |
DOC_USP7_MATH_1 | 72 | 76 | PF00917 | 0.517 |
DOC_USP7_UBL2_3 | 173 | 177 | PF12436 | 0.634 |
DOC_USP7_UBL2_3 | 179 | 183 | PF12436 | 0.545 |
DOC_USP7_UBL2_3 | 46 | 50 | PF12436 | 0.515 |
DOC_WW_Pin1_4 | 12 | 17 | PF00397 | 0.511 |
DOC_WW_Pin1_4 | 275 | 280 | PF00397 | 0.682 |
DOC_WW_Pin1_4 | 313 | 318 | PF00397 | 0.623 |
DOC_WW_Pin1_4 | 335 | 340 | PF00397 | 0.693 |
DOC_WW_Pin1_4 | 384 | 389 | PF00397 | 0.703 |
DOC_WW_Pin1_4 | 426 | 431 | PF00397 | 0.636 |
LIG_14-3-3_CanoR_1 | 143 | 149 | PF00244 | 0.556 |
LIG_14-3-3_CanoR_1 | 291 | 297 | PF00244 | 0.711 |
LIG_14-3-3_CanoR_1 | 419 | 423 | PF00244 | 0.592 |
LIG_Actin_WH2_2 | 5 | 21 | PF00022 | 0.555 |
LIG_FHA_1 | 2 | 8 | PF00498 | 0.533 |
LIG_FHA_1 | 240 | 246 | PF00498 | 0.560 |
LIG_FHA_1 | 449 | 455 | PF00498 | 0.586 |
LIG_FHA_2 | 305 | 311 | PF00498 | 0.643 |
LIG_FHA_2 | 78 | 84 | PF00498 | 0.532 |
LIG_GBD_Chelix_1 | 63 | 71 | PF00786 | 0.425 |
LIG_LIR_Gen_1 | 45 | 55 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 45 | 51 | PF02991 | 0.405 |
LIG_MYND_1 | 16 | 20 | PF01753 | 0.572 |
LIG_NRBOX | 1 | 7 | PF00104 | 0.534 |
LIG_PDZ_Class_2 | 452 | 457 | PF00595 | 0.654 |
LIG_RPA_C_Fungi | 97 | 109 | PF08784 | 0.464 |
LIG_SH2_STAT5 | 86 | 89 | PF00017 | 0.450 |
LIG_SH3_2 | 314 | 319 | PF14604 | 0.606 |
LIG_SH3_2 | 336 | 341 | PF14604 | 0.695 |
LIG_SH3_2 | 388 | 393 | PF14604 | 0.597 |
LIG_SH3_3 | 122 | 128 | PF00018 | 0.709 |
LIG_SH3_3 | 14 | 20 | PF00018 | 0.555 |
LIG_SH3_3 | 311 | 317 | PF00018 | 0.623 |
LIG_SH3_3 | 326 | 332 | PF00018 | 0.634 |
LIG_SH3_3 | 333 | 339 | PF00018 | 0.631 |
LIG_SH3_3 | 385 | 391 | PF00018 | 0.628 |
LIG_TRAF2_1 | 235 | 238 | PF00917 | 0.532 |
LIG_TRAF2_1 | 328 | 331 | PF00917 | 0.637 |
LIG_TRAF2_1 | 374 | 377 | PF00917 | 0.676 |
LIG_TRAF2_1 | 380 | 383 | PF00917 | 0.613 |
MOD_CDK_SPK_2 | 335 | 340 | PF00069 | 0.693 |
MOD_CDK_SPxK_1 | 313 | 319 | PF00069 | 0.603 |
MOD_CDK_SPxK_1 | 335 | 341 | PF00069 | 0.696 |
MOD_CDK_SPxxK_3 | 12 | 19 | PF00069 | 0.516 |
MOD_CDK_SPxxK_3 | 313 | 320 | PF00069 | 0.604 |
MOD_CDK_SPxxK_3 | 335 | 342 | PF00069 | 0.695 |
MOD_CK1_1 | 290 | 296 | PF00069 | 0.722 |
MOD_CK2_1 | 304 | 310 | PF00069 | 0.689 |
MOD_CK2_1 | 401 | 407 | PF00069 | 0.582 |
MOD_CK2_1 | 434 | 440 | PF00069 | 0.574 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.636 |
MOD_GlcNHglycan | 357 | 360 | PF01048 | 0.668 |
MOD_GlcNHglycan | 372 | 375 | PF01048 | 0.523 |
MOD_GlcNHglycan | 403 | 406 | PF01048 | 0.551 |
MOD_GlcNHglycan | 432 | 435 | PF01048 | 0.710 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.720 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.519 |
MOD_GSK3_1 | 351 | 358 | PF00069 | 0.706 |
MOD_GSK3_1 | 417 | 424 | PF00069 | 0.638 |
MOD_GSK3_1 | 426 | 433 | PF00069 | 0.643 |
MOD_N-GLC_1 | 297 | 302 | PF02516 | 0.676 |
MOD_N-GLC_1 | 449 | 454 | PF02516 | 0.559 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.614 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.553 |
MOD_NEK2_1 | 200 | 205 | PF00069 | 0.462 |
MOD_NEK2_1 | 51 | 56 | PF00069 | 0.438 |
MOD_PIKK_1 | 233 | 239 | PF00454 | 0.506 |
MOD_PIKK_1 | 290 | 296 | PF00454 | 0.681 |
MOD_PIKK_1 | 386 | 392 | PF00454 | 0.661 |
MOD_PIKK_1 | 54 | 60 | PF00454 | 0.347 |
MOD_PKA_1 | 334 | 340 | PF00069 | 0.666 |
MOD_PKA_2 | 290 | 296 | PF00069 | 0.722 |
MOD_PKA_2 | 418 | 424 | PF00069 | 0.653 |
MOD_PKB_1 | 342 | 350 | PF00069 | 0.661 |
MOD_Plk_1 | 200 | 206 | PF00069 | 0.499 |
MOD_ProDKin_1 | 12 | 18 | PF00069 | 0.513 |
MOD_ProDKin_1 | 275 | 281 | PF00069 | 0.684 |
MOD_ProDKin_1 | 313 | 319 | PF00069 | 0.626 |
MOD_ProDKin_1 | 335 | 341 | PF00069 | 0.696 |
MOD_ProDKin_1 | 384 | 390 | PF00069 | 0.703 |
MOD_ProDKin_1 | 426 | 432 | PF00069 | 0.633 |
MOD_SUMO_for_1 | 167 | 170 | PF00179 | 0.514 |
MOD_SUMO_for_1 | 178 | 181 | PF00179 | 0.481 |
MOD_SUMO_for_1 | 182 | 185 | PF00179 | 0.435 |
MOD_SUMO_for_1 | 188 | 191 | PF00179 | 0.439 |
MOD_SUMO_for_1 | 194 | 197 | PF00179 | 0.378 |
MOD_SUMO_rev_2 | 170 | 174 | PF00179 | 0.450 |
TRG_DiLeu_BaEn_1 | 244 | 249 | PF01217 | 0.529 |
TRG_ER_diArg_1 | 11 | 14 | PF00400 | 0.553 |
TRG_ER_diArg_1 | 204 | 207 | PF00400 | 0.535 |
TRG_ER_diArg_1 | 339 | 342 | PF00400 | 0.696 |
TRG_ER_diArg_1 | 36 | 38 | PF00400 | 0.481 |
TRG_ER_diArg_1 | 391 | 393 | PF00400 | 0.639 |
TRG_ER_diArg_1 | 67 | 69 | PF00400 | 0.428 |
TRG_ER_diArg_1 | 87 | 90 | PF00400 | 0.442 |
TRG_NLS_Bipartite_1 | 142 | 159 | PF00514 | 0.507 |
TRG_NLS_MonoExtN_4 | 154 | 159 | PF00514 | 0.541 |
TRG_Pf-PMV_PEXEL_1 | 216 | 220 | PF00026 | 0.482 |
TRG_Pf-PMV_PEXEL_1 | 61 | 65 | PF00026 | 0.447 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IUB2 | Leishmania donovani | 99% | 100% |
A4HM33 | Leishmania braziliensis | 53% | 98% |
E9B4G4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 77% | 100% |
Q4Q3L1 | Leishmania major | 88% | 100% |