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: A4IE65
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 56 | 60 | PF00656 | 0.668 |
CLV_NRD_NRD_1 | 133 | 135 | PF00675 | 0.534 |
CLV_NRD_NRD_1 | 237 | 239 | PF00675 | 0.675 |
CLV_NRD_NRD_1 | 333 | 335 | PF00675 | 0.639 |
CLV_NRD_NRD_1 | 390 | 392 | PF00675 | 0.557 |
CLV_NRD_NRD_1 | 396 | 398 | PF00675 | 0.549 |
CLV_NRD_NRD_1 | 85 | 87 | PF00675 | 0.498 |
CLV_PCSK_FUR_1 | 278 | 282 | PF00082 | 0.672 |
CLV_PCSK_KEX2_1 | 133 | 135 | PF00082 | 0.510 |
CLV_PCSK_KEX2_1 | 280 | 282 | PF00082 | 0.716 |
CLV_PCSK_KEX2_1 | 396 | 398 | PF00082 | 0.578 |
CLV_PCSK_KEX2_1 | 85 | 87 | PF00082 | 0.498 |
CLV_PCSK_PC1ET2_1 | 280 | 282 | PF00082 | 0.716 |
CLV_PCSK_SKI1_1 | 113 | 117 | PF00082 | 0.482 |
CLV_PCSK_SKI1_1 | 2 | 6 | PF00082 | 0.463 |
CLV_PCSK_SKI1_1 | 255 | 259 | PF00082 | 0.654 |
CLV_PCSK_SKI1_1 | 29 | 33 | PF00082 | 0.592 |
CLV_PCSK_SKI1_1 | 419 | 423 | PF00082 | 0.707 |
DEG_MDM2_SWIB_1 | 158 | 165 | PF02201 | 0.479 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.643 |
DEG_SPOP_SBC_1 | 191 | 195 | PF00917 | 0.604 |
DEG_SPOP_SBC_1 | 51 | 55 | PF00917 | 0.653 |
DOC_CYCLIN_RxL_1 | 252 | 261 | PF00134 | 0.630 |
DOC_CYCLIN_yCln2_LP_2 | 135 | 141 | PF00134 | 0.518 |
DOC_CYCLIN_yCln2_LP_2 | 31 | 34 | PF00134 | 0.583 |
DOC_MAPK_DCC_7 | 293 | 303 | PF00069 | 0.619 |
DOC_PP2B_LxvP_1 | 135 | 138 | PF13499 | 0.520 |
DOC_PP2B_LxvP_1 | 265 | 268 | PF13499 | 0.695 |
DOC_PP2B_LxvP_1 | 31 | 34 | PF13499 | 0.680 |
DOC_USP7_MATH_1 | 120 | 124 | PF00917 | 0.540 |
DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.472 |
DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.318 |
DOC_USP7_MATH_1 | 197 | 201 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 289 | 293 | PF00917 | 0.712 |
DOC_USP7_MATH_1 | 351 | 355 | PF00917 | 0.657 |
DOC_USP7_MATH_1 | 356 | 360 | PF00917 | 0.591 |
DOC_USP7_MATH_1 | 364 | 368 | PF00917 | 0.513 |
DOC_USP7_MATH_1 | 51 | 55 | PF00917 | 0.658 |
DOC_WW_Pin1_4 | 205 | 210 | PF00397 | 0.655 |
DOC_WW_Pin1_4 | 258 | 263 | PF00397 | 0.656 |
DOC_WW_Pin1_4 | 32 | 37 | PF00397 | 0.586 |
LIG_14-3-3_CanoR_1 | 113 | 122 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 255 | 261 | PF00244 | 0.630 |
LIG_14-3-3_CanoR_1 | 373 | 378 | PF00244 | 0.525 |
LIG_14-3-3_CanoR_1 | 86 | 92 | PF00244 | 0.513 |
LIG_BRCT_BRCA1_1 | 154 | 158 | PF00533 | 0.491 |
LIG_eIF4E_1 | 9 | 15 | PF01652 | 0.545 |
LIG_EVH1_2 | 68 | 72 | PF00568 | 0.580 |
LIG_FHA_1 | 10 | 16 | PF00498 | 0.556 |
LIG_FHA_1 | 114 | 120 | PF00498 | 0.574 |
LIG_FHA_1 | 17 | 23 | PF00498 | 0.488 |
LIG_FHA_1 | 298 | 304 | PF00498 | 0.593 |
LIG_FHA_2 | 184 | 190 | PF00498 | 0.543 |
LIG_FHA_2 | 35 | 41 | PF00498 | 0.527 |
LIG_FHA_2 | 54 | 60 | PF00498 | 0.520 |
LIG_LIR_Gen_1 | 155 | 166 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 155 | 161 | PF02991 | 0.485 |
LIG_NRBOX | 40 | 46 | PF00104 | 0.566 |
LIG_PCNA_yPIPBox_3 | 408 | 422 | PF02747 | 0.561 |
LIG_Pex14_2 | 127 | 131 | PF04695 | 0.491 |
LIG_Pex14_2 | 154 | 158 | PF04695 | 0.585 |
LIG_SH2_STAT3 | 149 | 152 | PF00017 | 0.490 |
LIG_SH2_STAT5 | 160 | 163 | PF00017 | 0.440 |
LIG_SH2_STAT5 | 276 | 279 | PF00017 | 0.653 |
LIG_SH2_STAT5 | 410 | 413 | PF00017 | 0.617 |
LIG_SH3_3 | 116 | 122 | PF00018 | 0.515 |
LIG_SH3_3 | 213 | 219 | PF00018 | 0.644 |
LIG_SH3_3 | 30 | 36 | PF00018 | 0.586 |
LIG_SH3_3 | 314 | 320 | PF00018 | 0.801 |
LIG_SH3_3 | 333 | 339 | PF00018 | 0.670 |
LIG_SUMO_SIM_anti_2 | 300 | 305 | PF11976 | 0.585 |
LIG_SUMO_SIM_par_1 | 256 | 261 | PF11976 | 0.629 |
LIG_SUMO_SIM_par_1 | 373 | 378 | PF11976 | 0.597 |
LIG_WW_3 | 214 | 218 | PF00397 | 0.567 |
MOD_CK1_1 | 192 | 198 | PF00069 | 0.595 |
MOD_CK1_1 | 205 | 211 | PF00069 | 0.568 |
MOD_CK1_1 | 354 | 360 | PF00069 | 0.667 |
MOD_CK1_1 | 362 | 368 | PF00069 | 0.559 |
MOD_CK1_1 | 73 | 79 | PF00069 | 0.508 |
MOD_CK1_1 | 8 | 14 | PF00069 | 0.594 |
MOD_CK2_1 | 34 | 40 | PF00069 | 0.531 |
MOD_CK2_1 | 417 | 423 | PF00069 | 0.516 |
MOD_Cter_Amidation | 278 | 281 | PF01082 | 0.721 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.723 |
MOD_GlcNHglycan | 220 | 223 | PF01048 | 0.611 |
MOD_GlcNHglycan | 241 | 244 | PF01048 | 0.712 |
MOD_GlcNHglycan | 248 | 251 | PF01048 | 0.630 |
MOD_GlcNHglycan | 287 | 290 | PF01048 | 0.660 |
MOD_GlcNHglycan | 293 | 296 | PF01048 | 0.602 |
MOD_GlcNHglycan | 330 | 333 | PF01048 | 0.698 |
MOD_GlcNHglycan | 370 | 373 | PF01048 | 0.580 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.577 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.557 |
MOD_GSK3_1 | 109 | 116 | PF00069 | 0.456 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.517 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.671 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.684 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.659 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.593 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.621 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.742 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.420 |
MOD_N-GLC_1 | 239 | 244 | PF02516 | 0.687 |
MOD_N-GLC_1 | 362 | 367 | PF02516 | 0.581 |
MOD_NEK2_1 | 114 | 119 | PF00069 | 0.514 |
MOD_NEK2_1 | 198 | 203 | PF00069 | 0.622 |
MOD_NEK2_1 | 220 | 225 | PF00069 | 0.743 |
MOD_NEK2_1 | 25 | 30 | PF00069 | 0.531 |
MOD_NEK2_1 | 45 | 50 | PF00069 | 0.697 |
MOD_NEK2_1 | 72 | 77 | PF00069 | 0.446 |
MOD_NEK2_2 | 139 | 144 | PF00069 | 0.515 |
MOD_NEK2_2 | 153 | 158 | PF00069 | 0.444 |
MOD_PK_1 | 373 | 379 | PF00069 | 0.461 |
MOD_PKA_2 | 198 | 204 | PF00069 | 0.578 |
MOD_Plk_1 | 16 | 22 | PF00069 | 0.496 |
MOD_Plk_4 | 153 | 159 | PF00069 | 0.451 |
MOD_Plk_4 | 95 | 101 | PF00069 | 0.495 |
MOD_ProDKin_1 | 205 | 211 | PF00069 | 0.655 |
MOD_ProDKin_1 | 258 | 264 | PF00069 | 0.654 |
MOD_ProDKin_1 | 32 | 38 | PF00069 | 0.584 |
MOD_SUMO_rev_2 | 174 | 182 | PF00179 | 0.592 |
TRG_DiLeu_BaEn_1 | 10 | 15 | PF01217 | 0.544 |
TRG_DiLeu_BaEn_1 | 178 | 183 | PF01217 | 0.538 |
TRG_DiLeu_BaEn_1 | 40 | 45 | PF01217 | 0.515 |
TRG_DiLeu_BaLyEn_6 | 167 | 172 | PF01217 | 0.568 |
TRG_DiLeu_BaLyEn_6 | 253 | 258 | PF01217 | 0.657 |
TRG_ER_diArg_1 | 133 | 135 | PF00400 | 0.510 |
TRG_ER_diArg_1 | 395 | 397 | PF00400 | 0.589 |
TRG_ER_diArg_1 | 85 | 87 | PF00400 | 0.498 |
TRG_Pf-PMV_PEXEL_1 | 180 | 184 | PF00026 | 0.653 |
TRG_Pf-PMV_PEXEL_1 | 373 | 378 | PF00026 | 0.539 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8ILA1 | Leishmania donovani | 99% | 100% |
A4HPS7 | Leishmania braziliensis | 70% | 100% |
E9ATJ2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
Q4Q106 | Leishmania major | 89% | 100% |