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: E9ANU4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 373 | 377 | PF00656 | 0.403 |
CLV_NRD_NRD_1 | 297 | 299 | PF00675 | 0.663 |
CLV_NRD_NRD_1 | 72 | 74 | PF00675 | 0.503 |
CLV_NRD_NRD_1 | 99 | 101 | PF00675 | 0.437 |
CLV_PCSK_KEX2_1 | 297 | 299 | PF00082 | 0.663 |
CLV_PCSK_KEX2_1 | 72 | 74 | PF00082 | 0.508 |
CLV_PCSK_KEX2_1 | 99 | 101 | PF00082 | 0.440 |
CLV_PCSK_PC7_1 | 95 | 101 | PF00082 | 0.371 |
CLV_PCSK_SKI1_1 | 239 | 243 | PF00082 | 0.554 |
CLV_PCSK_SKI1_1 | 284 | 288 | PF00082 | 0.495 |
DEG_APCC_DBOX_1 | 283 | 291 | PF00400 | 0.492 |
DEG_Nend_UBRbox_4 | 1 | 3 | PF02207 | 0.575 |
DEG_SPOP_SBC_1 | 157 | 161 | PF00917 | 0.547 |
DEG_SPOP_SBC_1 | 312 | 316 | PF00917 | 0.674 |
DOC_CYCLIN_RxL_1 | 99 | 112 | PF00134 | 0.528 |
DOC_MAPK_gen_1 | 180 | 187 | PF00069 | 0.591 |
DOC_MAPK_MEF2A_6 | 180 | 187 | PF00069 | 0.649 |
DOC_MAPK_RevD_3 | 283 | 298 | PF00069 | 0.635 |
DOC_USP7_MATH_1 | 103 | 107 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 128 | 132 | PF00917 | 0.534 |
DOC_USP7_MATH_1 | 157 | 161 | PF00917 | 0.693 |
DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.708 |
DOC_USP7_MATH_1 | 28 | 32 | PF00917 | 0.622 |
DOC_USP7_MATH_1 | 319 | 323 | PF00917 | 0.554 |
DOC_USP7_MATH_1 | 34 | 38 | PF00917 | 0.544 |
DOC_WW_Pin1_4 | 141 | 146 | PF00397 | 0.498 |
DOC_WW_Pin1_4 | 8 | 13 | PF00397 | 0.713 |
LIG_14-3-3_CanoR_1 | 105 | 110 | PF00244 | 0.391 |
LIG_14-3-3_CanoR_1 | 121 | 128 | PF00244 | 0.571 |
LIG_14-3-3_CanoR_1 | 297 | 303 | PF00244 | 0.564 |
LIG_14-3-3_CanoR_1 | 87 | 96 | PF00244 | 0.613 |
LIG_APCC_ABBA_1 | 206 | 211 | PF00400 | 0.482 |
LIG_BRCT_BRCA1_1 | 143 | 147 | PF00533 | 0.379 |
LIG_FHA_1 | 170 | 176 | PF00498 | 0.688 |
LIG_FHA_1 | 271 | 277 | PF00498 | 0.773 |
LIG_FHA_1 | 69 | 75 | PF00498 | 0.423 |
LIG_FHA_2 | 371 | 377 | PF00498 | 0.623 |
LIG_PDZ_Class_3 | 386 | 391 | PF00595 | 0.507 |
LIG_Pex14_2 | 147 | 151 | PF04695 | 0.362 |
LIG_SH2_STAP1 | 55 | 59 | PF00017 | 0.517 |
LIG_SH2_STAP1 | 61 | 65 | PF00017 | 0.502 |
LIG_SH2_STAP1 | 70 | 74 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 142 | 145 | PF00017 | 0.637 |
LIG_SH2_STAT5 | 230 | 233 | PF00017 | 0.636 |
LIG_SH2_STAT5 | 367 | 370 | PF00017 | 0.494 |
LIG_SH2_STAT5 | 379 | 382 | PF00017 | 0.326 |
LIG_SH2_STAT5 | 70 | 73 | PF00017 | 0.572 |
LIG_SH3_1 | 180 | 186 | PF00018 | 0.665 |
LIG_SH3_2 | 12 | 17 | PF14604 | 0.523 |
LIG_SH3_3 | 178 | 184 | PF00018 | 0.650 |
LIG_SH3_3 | 283 | 289 | PF00018 | 0.596 |
LIG_SH3_3 | 9 | 15 | PF00018 | 0.600 |
LIG_TRAF2_1 | 153 | 156 | PF00917 | 0.476 |
LIG_TRAF2_1 | 301 | 304 | PF00917 | 0.508 |
LIG_WW_2 | 183 | 186 | PF00397 | 0.569 |
MOD_CK1_1 | 131 | 137 | PF00069 | 0.599 |
MOD_CK1_1 | 158 | 164 | PF00069 | 0.630 |
MOD_CK1_1 | 24 | 30 | PF00069 | 0.747 |
MOD_CK1_1 | 308 | 314 | PF00069 | 0.686 |
MOD_CK1_1 | 371 | 377 | PF00069 | 0.545 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.637 |
MOD_CK1_1 | 76 | 82 | PF00069 | 0.442 |
MOD_CK1_1 | 83 | 89 | PF00069 | 0.481 |
MOD_CK2_1 | 170 | 176 | PF00069 | 0.516 |
MOD_CK2_1 | 298 | 304 | PF00069 | 0.566 |
MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.672 |
MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.524 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.664 |
MOD_GlcNHglycan | 216 | 220 | PF01048 | 0.503 |
MOD_GlcNHglycan | 23 | 26 | PF01048 | 0.647 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.534 |
MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.562 |
MOD_GlcNHglycan | 30 | 33 | PF01048 | 0.584 |
MOD_GlcNHglycan | 307 | 310 | PF01048 | 0.557 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.632 |
MOD_GlcNHglycan | 339 | 343 | PF01048 | 0.499 |
MOD_GlcNHglycan | 370 | 373 | PF01048 | 0.536 |
MOD_GlcNHglycan | 62 | 65 | PF01048 | 0.643 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.494 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.492 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.731 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.721 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.440 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.657 |
MOD_GSK3_1 | 308 | 315 | PF00069 | 0.750 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.448 |
MOD_N-GLC_1 | 271 | 276 | PF02516 | 0.720 |
MOD_N-GLC_1 | 68 | 73 | PF02516 | 0.457 |
MOD_NEK2_1 | 170 | 175 | PF00069 | 0.509 |
MOD_NEK2_1 | 270 | 275 | PF00069 | 0.517 |
MOD_NEK2_1 | 363 | 368 | PF00069 | 0.472 |
MOD_PIKK_1 | 122 | 128 | PF00454 | 0.549 |
MOD_PIKK_1 | 151 | 157 | PF00454 | 0.616 |
MOD_PIKK_1 | 87 | 93 | PF00454 | 0.605 |
MOD_PK_1 | 298 | 304 | PF00069 | 0.508 |
MOD_PKA_2 | 120 | 126 | PF00069 | 0.570 |
MOD_PKA_2 | 49 | 55 | PF00069 | 0.553 |
MOD_Plk_1 | 129 | 135 | PF00069 | 0.591 |
MOD_Plk_1 | 271 | 277 | PF00069 | 0.698 |
MOD_Plk_1 | 46 | 52 | PF00069 | 0.618 |
MOD_Plk_1 | 83 | 89 | PF00069 | 0.455 |
MOD_Plk_4 | 272 | 278 | PF00069 | 0.618 |
MOD_ProDKin_1 | 141 | 147 | PF00069 | 0.497 |
MOD_ProDKin_1 | 8 | 14 | PF00069 | 0.713 |
TRG_ENDOCYTIC_2 | 209 | 212 | PF00928 | 0.734 |
TRG_ER_diArg_1 | 179 | 182 | PF00400 | 0.612 |
TRG_ER_diArg_1 | 297 | 300 | PF00400 | 0.661 |
TRG_ER_diArg_1 | 72 | 75 | PF00400 | 0.501 |
TRG_NES_CRM1_1 | 339 | 352 | PF08389 | 0.365 |
TRG_Pf-PMV_PEXEL_1 | 72 | 77 | PF00026 | 0.564 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PD33 | Leptomonas seymouri | 30% | 84% |
A0A3S7WRT8 | Leishmania donovani | 75% | 98% |
A4H6T2 | Leishmania braziliensis | 58% | 100% |
E9AGA6 | Leishmania infantum | 75% | 98% |
Q4QGS6 | Leishmania major | 76% | 100% |