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: E9B458
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 124 | 128 | PF00656 | 0.647 |
CLV_C14_Caspase3-7 | 200 | 204 | PF00656 | 0.708 |
CLV_C14_Caspase3-7 | 327 | 331 | PF00656 | 0.606 |
CLV_C14_Caspase3-7 | 65 | 69 | PF00656 | 0.777 |
CLV_NRD_NRD_1 | 138 | 140 | PF00675 | 0.624 |
CLV_NRD_NRD_1 | 30 | 32 | PF00675 | 0.701 |
CLV_NRD_NRD_1 | 382 | 384 | PF00675 | 0.536 |
CLV_NRD_NRD_1 | 385 | 387 | PF00675 | 0.544 |
CLV_PCSK_KEX2_1 | 138 | 140 | PF00082 | 0.672 |
CLV_PCSK_KEX2_1 | 30 | 32 | PF00082 | 0.701 |
DEG_SCF_FBW7_2 | 348 | 354 | PF00400 | 0.505 |
DOC_ANK_TNKS_1 | 70 | 77 | PF00023 | 0.722 |
DOC_CKS1_1 | 348 | 353 | PF01111 | 0.505 |
DOC_USP7_MATH_1 | 165 | 169 | PF00917 | 0.682 |
DOC_USP7_MATH_1 | 315 | 319 | PF00917 | 0.737 |
DOC_USP7_MATH_1 | 58 | 62 | PF00917 | 0.588 |
DOC_WW_Pin1_4 | 146 | 151 | PF00397 | 0.827 |
DOC_WW_Pin1_4 | 161 | 166 | PF00397 | 0.592 |
DOC_WW_Pin1_4 | 229 | 234 | PF00397 | 0.695 |
DOC_WW_Pin1_4 | 347 | 352 | PF00397 | 0.555 |
LIG_14-3-3_CanoR_1 | 30 | 38 | PF00244 | 0.555 |
LIG_BIR_III_4 | 247 | 251 | PF00653 | 0.624 |
LIG_FHA_1 | 315 | 321 | PF00498 | 0.464 |
LIG_FHA_1 | 348 | 354 | PF00498 | 0.688 |
LIG_FHA_1 | 76 | 82 | PF00498 | 0.715 |
LIG_FHA_2 | 109 | 115 | PF00498 | 0.548 |
LIG_FHA_2 | 151 | 157 | PF00498 | 0.684 |
LIG_FHA_2 | 195 | 201 | PF00498 | 0.705 |
LIG_LIR_Gen_1 | 307 | 316 | PF02991 | 0.670 |
LIG_LIR_Gen_1 | 95 | 105 | PF02991 | 0.603 |
LIG_LIR_Nem_3 | 307 | 311 | PF02991 | 0.682 |
LIG_LIR_Nem_3 | 95 | 101 | PF02991 | 0.601 |
LIG_NRBOX | 177 | 183 | PF00104 | 0.713 |
LIG_REV1ctd_RIR_1 | 308 | 317 | PF16727 | 0.713 |
LIG_SH2_STAT5 | 281 | 284 | PF00017 | 0.422 |
LIG_SH2_STAT5 | 308 | 311 | PF00017 | 0.725 |
LIG_SH3_3 | 345 | 351 | PF00018 | 0.533 |
LIG_SUMO_SIM_par_1 | 58 | 65 | PF11976 | 0.515 |
LIG_TRAF2_1 | 197 | 200 | PF00917 | 0.702 |
LIG_TRAF2_1 | 93 | 96 | PF00917 | 0.734 |
LIG_WW_3 | 135 | 139 | PF00397 | 0.526 |
MOD_CDK_SPxxK_3 | 229 | 236 | PF00069 | 0.614 |
MOD_CK1_1 | 164 | 170 | PF00069 | 0.789 |
MOD_CK1_1 | 221 | 227 | PF00069 | 0.595 |
MOD_CK1_1 | 26 | 32 | PF00069 | 0.677 |
MOD_CK1_1 | 268 | 274 | PF00069 | 0.716 |
MOD_CK1_1 | 326 | 332 | PF00069 | 0.558 |
MOD_CK1_1 | 336 | 342 | PF00069 | 0.580 |
MOD_CK1_1 | 349 | 355 | PF00069 | 0.505 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.681 |
MOD_CK1_1 | 44 | 50 | PF00069 | 0.519 |
MOD_CK1_1 | 52 | 58 | PF00069 | 0.742 |
MOD_CK1_1 | 61 | 67 | PF00069 | 0.690 |
MOD_CK1_1 | 85 | 91 | PF00069 | 0.634 |
MOD_CK2_1 | 194 | 200 | PF00069 | 0.703 |
MOD_CK2_1 | 268 | 274 | PF00069 | 0.716 |
MOD_CK2_1 | 315 | 321 | PF00069 | 0.714 |
MOD_CK2_1 | 43 | 49 | PF00069 | 0.759 |
MOD_CK2_1 | 90 | 96 | PF00069 | 0.732 |
MOD_GlcNHglycan | 107 | 111 | PF01048 | 0.705 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.758 |
MOD_GlcNHglycan | 167 | 170 | PF01048 | 0.672 |
MOD_GlcNHglycan | 317 | 320 | PF01048 | 0.649 |
MOD_GlcNHglycan | 335 | 338 | PF01048 | 0.695 |
MOD_GlcNHglycan | 342 | 346 | PF01048 | 0.576 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.673 |
MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.586 |
MOD_GlcNHglycan | 87 | 90 | PF01048 | 0.712 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.783 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.707 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.744 |
MOD_GSK3_1 | 214 | 221 | PF00069 | 0.513 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.697 |
MOD_GSK3_1 | 332 | 339 | PF00069 | 0.593 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.645 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.573 |
MOD_GSK3_1 | 58 | 65 | PF00069 | 0.620 |
MOD_N-GLC_1 | 190 | 195 | PF02516 | 0.698 |
MOD_N-GLC_1 | 219 | 224 | PF02516 | 0.693 |
MOD_N-GLC_1 | 85 | 90 | PF02516 | 0.754 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.743 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.763 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.621 |
MOD_NEK2_1 | 235 | 240 | PF00069 | 0.544 |
MOD_NEK2_1 | 372 | 377 | PF00069 | 0.715 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.566 |
MOD_NEK2_2 | 306 | 311 | PF00069 | 0.659 |
MOD_PK_1 | 255 | 261 | PF00069 | 0.700 |
MOD_PKA_1 | 138 | 144 | PF00069 | 0.622 |
MOD_PKA_2 | 138 | 144 | PF00069 | 0.627 |
MOD_PKA_2 | 235 | 241 | PF00069 | 0.545 |
MOD_PKA_2 | 26 | 32 | PF00069 | 0.683 |
MOD_Plk_1 | 139 | 145 | PF00069 | 0.651 |
MOD_Plk_1 | 150 | 156 | PF00069 | 0.615 |
MOD_Plk_1 | 265 | 271 | PF00069 | 0.737 |
MOD_Plk_1 | 306 | 312 | PF00069 | 0.722 |
MOD_Plk_1 | 32 | 38 | PF00069 | 0.474 |
MOD_Plk_1 | 341 | 347 | PF00069 | 0.503 |
MOD_Plk_2-3 | 114 | 120 | PF00069 | 0.557 |
MOD_Plk_2-3 | 184 | 190 | PF00069 | 0.581 |
MOD_Plk_2-3 | 195 | 201 | PF00069 | 0.616 |
MOD_Plk_2-3 | 265 | 271 | PF00069 | 0.737 |
MOD_Plk_2-3 | 321 | 327 | PF00069 | 0.589 |
MOD_Plk_2-3 | 364 | 370 | PF00069 | 0.744 |
MOD_Plk_4 | 140 | 146 | PF00069 | 0.723 |
MOD_Plk_4 | 214 | 220 | PF00069 | 0.506 |
MOD_Plk_4 | 268 | 274 | PF00069 | 0.716 |
MOD_Plk_4 | 306 | 312 | PF00069 | 0.724 |
MOD_Plk_4 | 76 | 82 | PF00069 | 0.532 |
MOD_ProDKin_1 | 146 | 152 | PF00069 | 0.825 |
MOD_ProDKin_1 | 161 | 167 | PF00069 | 0.592 |
MOD_ProDKin_1 | 229 | 235 | PF00069 | 0.698 |
MOD_ProDKin_1 | 347 | 353 | PF00069 | 0.553 |
MOD_SUMO_for_1 | 296 | 299 | PF00179 | 0.502 |
MOD_SUMO_rev_2 | 114 | 122 | PF00179 | 0.654 |
MOD_SUMO_rev_2 | 247 | 256 | PF00179 | 0.703 |
TRG_ENDOCYTIC_2 | 308 | 311 | PF00928 | 0.678 |
TRG_ER_diArg_1 | 137 | 139 | PF00400 | 0.656 |
TRG_ER_diArg_1 | 14 | 17 | PF00400 | 0.539 |
TRG_NLS_MonoExtC_3 | 382 | 387 | PF00514 | 0.537 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S5H7U9 | Leishmania donovani | 80% | 100% |
A4HLT2 | Leishmania braziliensis | 54% | 100% |
A4I991 | Leishmania infantum | 80% | 100% |
Q4Q3W7 | Leishmania major | 77% | 100% |