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: Q4QBI2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 178 | 182 | PF00656 | 0.565 |
CLV_NRD_NRD_1 | 190 | 192 | PF00675 | 0.320 |
CLV_NRD_NRD_1 | 284 | 286 | PF00675 | 0.595 |
CLV_NRD_NRD_1 | 331 | 333 | PF00675 | 0.671 |
CLV_PCSK_KEX2_1 | 190 | 192 | PF00082 | 0.320 |
CLV_PCSK_KEX2_1 | 284 | 286 | PF00082 | 0.595 |
CLV_PCSK_PC7_1 | 186 | 192 | PF00082 | 0.393 |
CLV_PCSK_SKI1_1 | 190 | 194 | PF00082 | 0.393 |
CLV_PCSK_SKI1_1 | 267 | 271 | PF00082 | 0.596 |
CLV_PCSK_SKI1_1 | 284 | 288 | PF00082 | 0.594 |
CLV_PCSK_SKI1_1 | 293 | 297 | PF00082 | 0.515 |
DEG_APCC_DBOX_1 | 292 | 300 | PF00400 | 0.548 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.581 |
DOC_CDC14_PxL_1 | 117 | 125 | PF14671 | 0.593 |
DOC_CYCLIN_RxL_1 | 282 | 289 | PF00134 | 0.578 |
DOC_MAPK_gen_1 | 32 | 40 | PF00069 | 0.593 |
DOC_MAPK_MEF2A_6 | 32 | 40 | PF00069 | 0.593 |
DOC_MAPK_MEF2A_6 | 7 | 14 | PF00069 | 0.468 |
DOC_PP1_RVXF_1 | 319 | 326 | PF00149 | 0.624 |
DOC_USP7_MATH_1 | 137 | 141 | PF00917 | 0.593 |
DOC_USP7_MATH_1 | 151 | 155 | PF00917 | 0.427 |
DOC_USP7_MATH_1 | 196 | 200 | PF00917 | 0.608 |
DOC_USP7_MATH_1 | 214 | 218 | PF00917 | 0.277 |
DOC_USP7_MATH_1 | 380 | 384 | PF00917 | 0.525 |
DOC_USP7_MATH_1 | 58 | 62 | PF00917 | 0.576 |
DOC_WW_Pin1_4 | 286 | 291 | PF00397 | 0.583 |
LIG_14-3-3_CanoR_1 | 267 | 272 | PF00244 | 0.459 |
LIG_14-3-3_CanoR_1 | 326 | 331 | PF00244 | 0.551 |
LIG_Actin_WH2_2 | 270 | 286 | PF00022 | 0.577 |
LIG_Clathr_ClatBox_1 | 268 | 272 | PF01394 | 0.535 |
LIG_FHA_1 | 175 | 181 | PF00498 | 0.500 |
LIG_FHA_1 | 18 | 24 | PF00498 | 0.457 |
LIG_FHA_1 | 268 | 274 | PF00498 | 0.594 |
LIG_FHA_1 | 278 | 284 | PF00498 | 0.499 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.495 |
LIG_FHA_2 | 143 | 149 | PF00498 | 0.593 |
LIG_FXI_DFP_1 | 362 | 366 | PF00024 | 0.596 |
LIG_LIR_Nem_3 | 210 | 215 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 335 | 339 | PF02991 | 0.527 |
LIG_Pex14_2 | 361 | 365 | PF04695 | 0.594 |
LIG_PTB_Apo_2 | 170 | 177 | PF02174 | 0.565 |
LIG_PTB_Phospho_1 | 170 | 176 | PF10480 | 0.565 |
LIG_SH2_NCK_1 | 238 | 242 | PF00017 | 0.657 |
LIG_SH2_NCK_1 | 99 | 103 | PF00017 | 0.537 |
LIG_SH2_PTP2 | 343 | 346 | PF00017 | 0.629 |
LIG_SH2_STAP1 | 176 | 180 | PF00017 | 0.568 |
LIG_SH2_STAT5 | 176 | 179 | PF00017 | 0.565 |
LIG_SH2_STAT5 | 206 | 209 | PF00017 | 0.490 |
LIG_SH2_STAT5 | 212 | 215 | PF00017 | 0.440 |
LIG_SH2_STAT5 | 305 | 308 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 343 | 346 | PF00017 | 0.629 |
LIG_SH3_1 | 25 | 31 | PF00018 | 0.537 |
LIG_SH3_3 | 104 | 110 | PF00018 | 0.565 |
LIG_SH3_3 | 25 | 31 | PF00018 | 0.537 |
LIG_SH3_3 | 336 | 342 | PF00018 | 0.548 |
LIG_SUMO_SIM_anti_2 | 154 | 159 | PF11976 | 0.587 |
LIG_SUMO_SIM_par_1 | 139 | 146 | PF11976 | 0.572 |
LIG_TRAF2_1 | 253 | 256 | PF00917 | 0.686 |
LIG_TRAF2_1 | 31 | 34 | PF00917 | 0.593 |
LIG_TYR_ITIM | 334 | 339 | PF00017 | 0.627 |
LIG_UBA3_1 | 26 | 35 | PF00899 | 0.487 |
LIG_UBA3_1 | 268 | 276 | PF00899 | 0.523 |
LIG_WRC_WIRS_1 | 230 | 235 | PF05994 | 0.481 |
LIG_WRC_WIRS_1 | 245 | 250 | PF05994 | 0.555 |
MOD_CDK_SPxxK_3 | 286 | 293 | PF00069 | 0.542 |
MOD_CK1_1 | 140 | 146 | PF00069 | 0.389 |
MOD_CK1_1 | 17 | 23 | PF00069 | 0.487 |
MOD_CK1_1 | 314 | 320 | PF00069 | 0.629 |
MOD_CK1_1 | 56 | 62 | PF00069 | 0.487 |
MOD_CK2_1 | 97 | 103 | PF00069 | 0.464 |
MOD_GlcNHglycan | 16 | 19 | PF01048 | 0.487 |
MOD_GlcNHglycan | 306 | 309 | PF01048 | 0.481 |
MOD_GlcNHglycan | 310 | 316 | PF01048 | 0.554 |
MOD_GlcNHglycan | 350 | 353 | PF01048 | 0.568 |
MOD_GlcNHglycan | 378 | 381 | PF01048 | 0.517 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.483 |
MOD_GlcNHglycan | 62 | 65 | PF01048 | 0.375 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.210 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.447 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.382 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.487 |
MOD_GSK3_1 | 376 | 383 | PF00069 | 0.583 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.437 |
MOD_N-GLC_1 | 59 | 64 | PF02516 | 0.409 |
MOD_NEK2_1 | 14 | 19 | PF00069 | 0.445 |
MOD_NEK2_1 | 142 | 147 | PF00069 | 0.473 |
MOD_NEK2_1 | 365 | 370 | PF00069 | 0.461 |
MOD_PIKK_1 | 277 | 283 | PF00454 | 0.440 |
MOD_PKA_2 | 348 | 354 | PF00069 | 0.545 |
MOD_Plk_1 | 180 | 186 | PF00069 | 0.493 |
MOD_Plk_4 | 137 | 143 | PF00069 | 0.394 |
MOD_Plk_4 | 18 | 24 | PF00069 | 0.487 |
MOD_Plk_4 | 180 | 186 | PF00069 | 0.379 |
MOD_Plk_4 | 214 | 220 | PF00069 | 0.555 |
MOD_Plk_4 | 229 | 235 | PF00069 | 0.533 |
MOD_Plk_4 | 97 | 103 | PF00069 | 0.372 |
MOD_ProDKin_1 | 286 | 292 | PF00069 | 0.576 |
TRG_DiLeu_BaEn_3 | 256 | 262 | PF01217 | 0.453 |
TRG_DiLeu_BaEn_3 | 33 | 39 | PF01217 | 0.487 |
TRG_DiLeu_BaLyEn_6 | 22 | 27 | PF01217 | 0.409 |
TRG_ENDOCYTIC_2 | 212 | 215 | PF00928 | 0.447 |
TRG_ENDOCYTIC_2 | 336 | 339 | PF00928 | 0.521 |
TRG_ENDOCYTIC_2 | 343 | 346 | PF00928 | 0.527 |
TRG_ENDOCYTIC_2 | 99 | 102 | PF00928 | 0.385 |
TRG_ER_diArg_1 | 189 | 191 | PF00400 | 0.385 |
TRG_ER_diArg_1 | 283 | 285 | PF00400 | 0.592 |
TRG_NES_CRM1_1 | 260 | 272 | PF08389 | 0.407 |
TRG_Pf-PMV_PEXEL_1 | 190 | 194 | PF00026 | 0.487 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4J8A6 | Bodo saltans | 27% | 100% |
A0A3Q8ILT9 | Leishmania donovani | 94% | 100% |
A4HCK6 | Leishmania braziliensis | 83% | 95% |
A4I024 | Leishmania infantum | 94% | 100% |
E9AVZ7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
P31521 | Pseudomonas chlororaphis | 27% | 92% |
P94400 | Bacillus subtilis (strain 168) | 26% | 97% |