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: E9AV73
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 273 | 277 | PF00656 | 0.568 |
CLV_C14_Caspase3-7 | 83 | 87 | PF00656 | 0.533 |
CLV_NRD_NRD_1 | 13 | 15 | PF00675 | 0.582 |
CLV_NRD_NRD_1 | 327 | 329 | PF00675 | 0.543 |
CLV_NRD_NRD_1 | 54 | 56 | PF00675 | 0.657 |
CLV_PCSK_KEX2_1 | 13 | 15 | PF00082 | 0.587 |
CLV_PCSK_KEX2_1 | 209 | 211 | PF00082 | 0.631 |
CLV_PCSK_KEX2_1 | 326 | 328 | PF00082 | 0.544 |
CLV_PCSK_KEX2_1 | 54 | 56 | PF00082 | 0.657 |
CLV_PCSK_PC1ET2_1 | 209 | 211 | PF00082 | 0.631 |
CLV_PCSK_SKI1_1 | 108 | 112 | PF00082 | 0.547 |
CLV_PCSK_SKI1_1 | 255 | 259 | PF00082 | 0.644 |
CLV_PCSK_SKI1_1 | 321 | 325 | PF00082 | 0.484 |
CLV_PCSK_SKI1_1 | 390 | 394 | PF00082 | 0.610 |
DEG_APCC_DBOX_1 | 103 | 111 | PF00400 | 0.653 |
DEG_APCC_DBOX_1 | 235 | 243 | PF00400 | 0.647 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.590 |
DOC_CYCLIN_RxL_1 | 163 | 171 | PF00134 | 0.624 |
DOC_MAPK_MEF2A_6 | 355 | 364 | PF00069 | 0.488 |
DOC_PP1_RVXF_1 | 164 | 171 | PF00149 | 0.571 |
DOC_PP2B_LxvP_1 | 115 | 118 | PF13499 | 0.494 |
DOC_USP7_MATH_1 | 149 | 153 | PF00917 | 0.555 |
DOC_USP7_MATH_1 | 24 | 28 | PF00917 | 0.635 |
DOC_USP7_MATH_1 | 250 | 254 | PF00917 | 0.601 |
DOC_USP7_MATH_1 | 275 | 279 | PF00917 | 0.686 |
DOC_USP7_MATH_1 | 287 | 291 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 344 | 348 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 56 | 60 | PF00917 | 0.593 |
DOC_USP7_MATH_1 | 61 | 65 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 82 | 86 | PF00917 | 0.491 |
DOC_WW_Pin1_4 | 191 | 196 | PF00397 | 0.627 |
DOC_WW_Pin1_4 | 20 | 25 | PF00397 | 0.533 |
DOC_WW_Pin1_4 | 283 | 288 | PF00397 | 0.584 |
DOC_WW_Pin1_4 | 348 | 353 | PF00397 | 0.462 |
LIG_14-3-3_CanoR_1 | 14 | 24 | PF00244 | 0.591 |
LIG_14-3-3_CanoR_1 | 143 | 150 | PF00244 | 0.526 |
LIG_14-3-3_CanoR_1 | 255 | 265 | PF00244 | 0.601 |
LIG_14-3-3_CanoR_1 | 390 | 398 | PF00244 | 0.602 |
LIG_14-3-3_CanoR_1 | 72 | 76 | PF00244 | 0.466 |
LIG_FHA_1 | 119 | 125 | PF00498 | 0.594 |
LIG_FHA_1 | 149 | 155 | PF00498 | 0.587 |
LIG_FHA_1 | 157 | 163 | PF00498 | 0.604 |
LIG_FHA_1 | 75 | 81 | PF00498 | 0.565 |
LIG_FHA_2 | 137 | 143 | PF00498 | 0.581 |
LIG_FHA_2 | 271 | 277 | PF00498 | 0.583 |
LIG_FHA_2 | 297 | 303 | PF00498 | 0.568 |
LIG_LIR_Gen_1 | 312 | 320 | PF02991 | 0.458 |
LIG_LIR_Gen_1 | 369 | 379 | PF02991 | 0.652 |
LIG_LIR_Gen_1 | 411 | 415 | PF02991 | 0.570 |
LIG_LIR_Nem_3 | 181 | 185 | PF02991 | 0.548 |
LIG_LIR_Nem_3 | 199 | 204 | PF02991 | 0.655 |
LIG_LIR_Nem_3 | 253 | 257 | PF02991 | 0.595 |
LIG_LIR_Nem_3 | 312 | 316 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 369 | 375 | PF02991 | 0.520 |
LIG_LIR_Nem_3 | 411 | 415 | PF02991 | 0.570 |
LIG_MYND_1 | 289 | 293 | PF01753 | 0.641 |
LIG_NRBOX | 106 | 112 | PF00104 | 0.492 |
LIG_PCNA_PIPBox_1 | 100 | 109 | PF02747 | 0.536 |
LIG_PCNA_yPIPBox_3 | 317 | 328 | PF02747 | 0.487 |
LIG_SH2_CRK | 201 | 205 | PF00017 | 0.523 |
LIG_SH2_PTP2 | 313 | 316 | PF00017 | 0.510 |
LIG_SH2_SRC | 309 | 312 | PF00017 | 0.545 |
LIG_SH2_STAP1 | 333 | 337 | PF00017 | 0.585 |
LIG_SH2_STAP1 | 372 | 376 | PF00017 | 0.521 |
LIG_SH2_STAT5 | 167 | 170 | PF00017 | 0.631 |
LIG_SH2_STAT5 | 309 | 312 | PF00017 | 0.490 |
LIG_SH2_STAT5 | 313 | 316 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 333 | 336 | PF00017 | 0.569 |
LIG_SH2_STAT5 | 94 | 97 | PF00017 | 0.555 |
LIG_SH3_3 | 279 | 285 | PF00018 | 0.621 |
LIG_SH3_3 | 286 | 292 | PF00018 | 0.579 |
LIG_SH3_3 | 346 | 352 | PF00018 | 0.596 |
LIG_SH3_3 | 359 | 365 | PF00018 | 0.449 |
LIG_SH3_3 | 87 | 93 | PF00018 | 0.546 |
LIG_SH3_5 | 329 | 333 | PF00018 | 0.594 |
MOD_CDK_SPxxK_3 | 348 | 355 | PF00069 | 0.455 |
MOD_CK1_1 | 136 | 142 | PF00069 | 0.624 |
MOD_CK1_1 | 189 | 195 | PF00069 | 0.625 |
MOD_CK1_1 | 270 | 276 | PF00069 | 0.646 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.598 |
MOD_CK1_1 | 71 | 77 | PF00069 | 0.520 |
MOD_CK2_1 | 296 | 302 | PF00069 | 0.521 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.549 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.465 |
MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.634 |
MOD_GlcNHglycan | 26 | 29 | PF01048 | 0.697 |
MOD_GlcNHglycan | 265 | 268 | PF01048 | 0.729 |
MOD_GlcNHglycan | 269 | 272 | PF01048 | 0.577 |
MOD_GlcNHglycan | 278 | 281 | PF01048 | 0.642 |
MOD_GlcNHglycan | 338 | 341 | PF01048 | 0.511 |
MOD_GlcNHglycan | 65 | 68 | PF01048 | 0.642 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.575 |
MOD_GlcNHglycan | 86 | 89 | PF01048 | 0.560 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.654 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.589 |
MOD_GSK3_1 | 263 | 270 | PF00069 | 0.688 |
MOD_GSK3_1 | 283 | 290 | PF00069 | 0.744 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.494 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.741 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.640 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.616 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.520 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.607 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.568 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.625 |
MOD_NEK2_1 | 168 | 173 | PF00069 | 0.696 |
MOD_NEK2_1 | 269 | 274 | PF00069 | 0.504 |
MOD_NEK2_1 | 39 | 44 | PF00069 | 0.620 |
MOD_NEK2_1 | 402 | 407 | PF00069 | 0.653 |
MOD_NEK2_1 | 5 | 10 | PF00069 | 0.536 |
MOD_NEK2_1 | 60 | 65 | PF00069 | 0.626 |
MOD_NEK2_2 | 250 | 255 | PF00069 | 0.599 |
MOD_PIKK_1 | 156 | 162 | PF00454 | 0.588 |
MOD_PIKK_1 | 384 | 390 | PF00454 | 0.500 |
MOD_PKA_1 | 327 | 333 | PF00069 | 0.531 |
MOD_PKA_2 | 142 | 148 | PF00069 | 0.522 |
MOD_PKA_2 | 15 | 21 | PF00069 | 0.682 |
MOD_PKA_2 | 261 | 267 | PF00069 | 0.488 |
MOD_PKA_2 | 327 | 333 | PF00069 | 0.531 |
MOD_PKA_2 | 5 | 11 | PF00069 | 0.607 |
MOD_PKA_2 | 71 | 77 | PF00069 | 0.458 |
MOD_Plk_1 | 186 | 192 | PF00069 | 0.476 |
MOD_Plk_4 | 186 | 192 | PF00069 | 0.538 |
MOD_Plk_4 | 221 | 227 | PF00069 | 0.713 |
MOD_Plk_4 | 230 | 236 | PF00069 | 0.584 |
MOD_Plk_4 | 296 | 302 | PF00069 | 0.521 |
MOD_Plk_4 | 305 | 311 | PF00069 | 0.494 |
MOD_ProDKin_1 | 191 | 197 | PF00069 | 0.629 |
MOD_ProDKin_1 | 20 | 26 | PF00069 | 0.530 |
MOD_ProDKin_1 | 283 | 289 | PF00069 | 0.581 |
MOD_ProDKin_1 | 348 | 354 | PF00069 | 0.458 |
TRG_DiLeu_BaLyEn_6 | 111 | 116 | PF01217 | 0.560 |
TRG_DiLeu_LyEn_5 | 241 | 246 | PF01217 | 0.604 |
TRG_ENDOCYTIC_2 | 167 | 170 | PF00928 | 0.631 |
TRG_ENDOCYTIC_2 | 201 | 204 | PF00928 | 0.667 |
TRG_ENDOCYTIC_2 | 313 | 316 | PF00928 | 0.510 |
TRG_ENDOCYTIC_2 | 372 | 375 | PF00928 | 0.468 |
TRG_ENDOCYTIC_2 | 412 | 415 | PF00928 | 0.575 |
TRG_ER_diArg_1 | 13 | 16 | PF00400 | 0.766 |
TRG_ER_diArg_1 | 325 | 328 | PF00400 | 0.547 |
TRG_Pf-PMV_PEXEL_1 | 108 | 113 | PF00026 | 0.550 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDR9 | Leptomonas seymouri | 37% | 93% |
A0A3Q8IAW3 | Leishmania donovani | 82% | 98% |
E9AGV7 | Leishmania infantum | 82% | 98% |
Q4QCA8 | Leishmania major | 80% | 100% |