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: E9B6T2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 298 | 302 | PF00656 | 0.509 |
CLV_C14_Caspase3-7 | 46 | 50 | PF00656 | 0.607 |
CLV_NRD_NRD_1 | 101 | 103 | PF00675 | 0.397 |
CLV_NRD_NRD_1 | 119 | 121 | PF00675 | 0.464 |
CLV_NRD_NRD_1 | 21 | 23 | PF00675 | 0.361 |
CLV_NRD_NRD_1 | 218 | 220 | PF00675 | 0.634 |
CLV_NRD_NRD_1 | 295 | 297 | PF00675 | 0.644 |
CLV_NRD_NRD_1 | 347 | 349 | PF00675 | 0.569 |
CLV_PCSK_FUR_1 | 274 | 278 | PF00082 | 0.648 |
CLV_PCSK_FUR_1 | 345 | 349 | PF00082 | 0.563 |
CLV_PCSK_KEX2_1 | 101 | 103 | PF00082 | 0.397 |
CLV_PCSK_KEX2_1 | 119 | 121 | PF00082 | 0.464 |
CLV_PCSK_KEX2_1 | 125 | 127 | PF00082 | 0.516 |
CLV_PCSK_KEX2_1 | 21 | 23 | PF00082 | 0.348 |
CLV_PCSK_KEX2_1 | 218 | 220 | PF00082 | 0.675 |
CLV_PCSK_KEX2_1 | 25 | 27 | PF00082 | 0.303 |
CLV_PCSK_KEX2_1 | 276 | 278 | PF00082 | 0.648 |
CLV_PCSK_KEX2_1 | 295 | 297 | PF00082 | 0.587 |
CLV_PCSK_KEX2_1 | 347 | 349 | PF00082 | 0.690 |
CLV_PCSK_PC1ET2_1 | 125 | 127 | PF00082 | 0.523 |
CLV_PCSK_PC1ET2_1 | 25 | 27 | PF00082 | 0.404 |
CLV_PCSK_PC1ET2_1 | 276 | 278 | PF00082 | 0.633 |
CLV_PCSK_PC7_1 | 21 | 27 | PF00082 | 0.304 |
CLV_PCSK_SKI1_1 | 21 | 25 | PF00082 | 0.347 |
CLV_PCSK_SKI1_1 | 26 | 30 | PF00082 | 0.311 |
CLV_PCSK_SKI1_1 | 381 | 385 | PF00082 | 0.490 |
CLV_PCSK_SKI1_1 | 54 | 58 | PF00082 | 0.555 |
CLV_PCSK_SKI1_1 | 84 | 88 | PF00082 | 0.417 |
DEG_APCC_DBOX_1 | 100 | 108 | PF00400 | 0.402 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.432 |
DEG_SPOP_SBC_1 | 318 | 322 | PF00917 | 0.618 |
DOC_ANK_TNKS_1 | 177 | 184 | PF00023 | 0.559 |
DOC_MAPK_gen_1 | 21 | 31 | PF00069 | 0.369 |
DOC_MAPK_MEF2A_6 | 22 | 31 | PF00069 | 0.376 |
DOC_PP1_RVXF_1 | 379 | 385 | PF00149 | 0.479 |
DOC_PP4_FxxP_1 | 257 | 260 | PF00568 | 0.651 |
DOC_PP4_FxxP_1 | 384 | 387 | PF00568 | 0.532 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.369 |
DOC_USP7_MATH_1 | 182 | 186 | PF00917 | 0.509 |
DOC_USP7_MATH_1 | 205 | 209 | PF00917 | 0.528 |
DOC_USP7_MATH_1 | 260 | 264 | PF00917 | 0.616 |
DOC_USP7_MATH_1 | 341 | 345 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 65 | 69 | PF00917 | 0.550 |
DOC_USP7_MATH_1 | 75 | 79 | PF00917 | 0.577 |
DOC_WW_Pin1_4 | 153 | 158 | PF00397 | 0.542 |
DOC_WW_Pin1_4 | 203 | 208 | PF00397 | 0.616 |
LIG_14-3-3_CanoR_1 | 160 | 166 | PF00244 | 0.611 |
LIG_14-3-3_CanoR_1 | 254 | 260 | PF00244 | 0.742 |
LIG_14-3-3_CanoR_1 | 287 | 297 | PF00244 | 0.632 |
LIG_14-3-3_CanoR_1 | 351 | 355 | PF00244 | 0.821 |
LIG_BIR_III_4 | 243 | 247 | PF00653 | 0.548 |
LIG_BRCT_BRCA1_1 | 321 | 325 | PF00533 | 0.611 |
LIG_BRCT_BRCA1_1 | 82 | 86 | PF00533 | 0.617 |
LIG_CtBP_PxDLS_1 | 192 | 196 | PF00389 | 0.529 |
LIG_FHA_1 | 377 | 383 | PF00498 | 0.466 |
LIG_FHA_1 | 43 | 49 | PF00498 | 0.652 |
LIG_LIR_Gen_1 | 106 | 115 | PF02991 | 0.606 |
LIG_LIR_Gen_1 | 162 | 173 | PF02991 | 0.536 |
LIG_LIR_Gen_1 | 4 | 13 | PF02991 | 0.304 |
LIG_LIR_Gen_1 | 83 | 93 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 106 | 112 | PF02991 | 0.601 |
LIG_LIR_Nem_3 | 4 | 9 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 83 | 89 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 91 | 96 | PF02991 | 0.407 |
LIG_MYND_1 | 207 | 211 | PF01753 | 0.628 |
LIG_SH2_STAP1 | 105 | 109 | PF00017 | 0.410 |
LIG_SH2_STAT3 | 370 | 373 | PF00017 | 0.472 |
LIG_SH2_STAT5 | 103 | 106 | PF00017 | 0.421 |
LIG_SH3_3 | 181 | 187 | PF00018 | 0.689 |
LIG_SH3_3 | 201 | 207 | PF00018 | 0.619 |
LIG_SH3_3 | 335 | 341 | PF00018 | 0.647 |
LIG_SH3_3 | 361 | 367 | PF00018 | 0.609 |
LIG_TRAF2_1 | 16 | 19 | PF00917 | 0.369 |
LIG_TRAF2_1 | 41 | 44 | PF00917 | 0.467 |
MOD_CDK_SPxxK_3 | 153 | 160 | PF00069 | 0.552 |
MOD_CK1_1 | 203 | 209 | PF00069 | 0.653 |
MOD_CK1_1 | 233 | 239 | PF00069 | 0.487 |
MOD_CK2_1 | 13 | 19 | PF00069 | 0.304 |
MOD_CK2_1 | 163 | 169 | PF00069 | 0.590 |
MOD_CK2_1 | 334 | 340 | PF00069 | 0.588 |
MOD_Cter_Amidation | 274 | 277 | PF01082 | 0.512 |
MOD_Cter_Amidation | 345 | 348 | PF01082 | 0.558 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.468 |
MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.509 |
MOD_GlcNHglycan | 243 | 247 | PF01048 | 0.766 |
MOD_GlcNHglycan | 297 | 300 | PF01048 | 0.570 |
MOD_GlcNHglycan | 321 | 324 | PF01048 | 0.527 |
MOD_GlcNHglycan | 340 | 344 | PF01048 | 0.618 |
MOD_GlcNHglycan | 352 | 355 | PF01048 | 0.529 |
MOD_GlcNHglycan | 37 | 40 | PF01048 | 0.492 |
MOD_GlcNHglycan | 63 | 66 | PF01048 | 0.686 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.651 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.599 |
MOD_GSK3_1 | 282 | 289 | PF00069 | 0.638 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.630 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.581 |
MOD_GSK3_1 | 372 | 379 | PF00069 | 0.453 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.555 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.426 |
MOD_N-GLC_1 | 61 | 66 | PF02516 | 0.567 |
MOD_NEK2_1 | 168 | 173 | PF00069 | 0.523 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.627 |
MOD_NEK2_1 | 309 | 314 | PF00069 | 0.589 |
MOD_NEK2_1 | 317 | 322 | PF00069 | 0.654 |
MOD_PIKK_1 | 248 | 254 | PF00454 | 0.648 |
MOD_PIKK_1 | 288 | 294 | PF00454 | 0.661 |
MOD_PKA_1 | 295 | 301 | PF00069 | 0.678 |
MOD_PKA_2 | 159 | 165 | PF00069 | 0.550 |
MOD_PKA_2 | 286 | 292 | PF00069 | 0.600 |
MOD_PKA_2 | 295 | 301 | PF00069 | 0.564 |
MOD_PKA_2 | 350 | 356 | PF00069 | 0.657 |
MOD_Plk_1 | 168 | 174 | PF00069 | 0.545 |
MOD_Plk_1 | 199 | 205 | PF00069 | 0.528 |
MOD_Plk_1 | 309 | 315 | PF00069 | 0.476 |
MOD_Plk_1 | 376 | 382 | PF00069 | 0.459 |
MOD_Plk_1 | 43 | 49 | PF00069 | 0.498 |
MOD_Plk_1 | 65 | 71 | PF00069 | 0.546 |
MOD_Plk_2-3 | 44 | 50 | PF00069 | 0.483 |
MOD_Plk_4 | 334 | 340 | PF00069 | 0.573 |
MOD_ProDKin_1 | 153 | 159 | PF00069 | 0.546 |
MOD_ProDKin_1 | 203 | 209 | PF00069 | 0.617 |
TRG_ENDOCYTIC_2 | 109 | 112 | PF00928 | 0.607 |
TRG_ENDOCYTIC_2 | 5 | 8 | PF00928 | 0.304 |
TRG_ENDOCYTIC_2 | 93 | 96 | PF00928 | 0.374 |
TRG_ER_diArg_1 | 101 | 103 | PF00400 | 0.397 |
TRG_ER_diArg_1 | 20 | 22 | PF00400 | 0.334 |
TRG_ER_diArg_1 | 218 | 220 | PF00400 | 0.569 |
TRG_ER_diArg_1 | 295 | 297 | PF00400 | 0.757 |
TRG_ER_diArg_1 | 345 | 348 | PF00400 | 0.558 |
TRG_NES_CRM1_1 | 18 | 30 | PF08389 | 0.369 |
TRG_Pf-PMV_PEXEL_1 | 102 | 106 | PF00026 | 0.392 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBL0 | Leptomonas seymouri | 31% | 100% |
A0A3Q8IIN7 | Leishmania donovani | 82% | 100% |
A4HN74 | Leishmania braziliensis | 66% | 100% |
A4IBU2 | Leishmania infantum | 81% | 100% |
E9AFM9 | Leishmania major | 81% | 99% |