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: A0A3S7WV66
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 16 | 20 | PF00656 | 0.530 |
CLV_NRD_NRD_1 | 175 | 177 | PF00675 | 0.436 |
CLV_NRD_NRD_1 | 201 | 203 | PF00675 | 0.432 |
CLV_NRD_NRD_1 | 204 | 206 | PF00675 | 0.427 |
CLV_NRD_NRD_1 | 247 | 249 | PF00675 | 0.641 |
CLV_NRD_NRD_1 | 388 | 390 | PF00675 | 0.549 |
CLV_PCSK_FUR_1 | 202 | 206 | PF00082 | 0.420 |
CLV_PCSK_KEX2_1 | 175 | 177 | PF00082 | 0.436 |
CLV_PCSK_KEX2_1 | 201 | 203 | PF00082 | 0.432 |
CLV_PCSK_KEX2_1 | 204 | 206 | PF00082 | 0.427 |
CLV_PCSK_KEX2_1 | 247 | 249 | PF00082 | 0.643 |
CLV_PCSK_KEX2_1 | 40 | 42 | PF00082 | 0.400 |
CLV_PCSK_PC1ET2_1 | 40 | 42 | PF00082 | 0.388 |
CLV_PCSK_SKI1_1 | 165 | 169 | PF00082 | 0.524 |
CLV_PCSK_SKI1_1 | 247 | 251 | PF00082 | 0.648 |
CLV_PCSK_SKI1_1 | 376 | 380 | PF00082 | 0.537 |
CLV_PCSK_SKI1_1 | 40 | 44 | PF00082 | 0.400 |
CLV_PCSK_SKI1_1 | 77 | 81 | PF00082 | 0.291 |
DEG_SPOP_SBC_1 | 361 | 365 | PF00917 | 0.524 |
DOC_CDC14_PxL_1 | 207 | 215 | PF14671 | 0.498 |
DOC_CYCLIN_RxL_1 | 245 | 252 | PF00134 | 0.586 |
DOC_MAPK_gen_1 | 175 | 182 | PF00069 | 0.383 |
DOC_MAPK_MEF2A_6 | 175 | 184 | PF00069 | 0.374 |
DOC_PP1_RVXF_1 | 33 | 39 | PF00149 | 0.283 |
DOC_USP7_MATH_1 | 218 | 222 | PF00917 | 0.441 |
DOC_USP7_MATH_1 | 225 | 229 | PF00917 | 0.516 |
DOC_USP7_MATH_1 | 260 | 264 | PF00917 | 0.644 |
DOC_USP7_MATH_1 | 360 | 364 | PF00917 | 0.647 |
DOC_USP7_MATH_1 | 367 | 371 | PF00917 | 0.494 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.652 |
DOC_USP7_MATH_1 | 62 | 66 | PF00917 | 0.294 |
DOC_USP7_MATH_1 | 94 | 98 | PF00917 | 0.490 |
DOC_WW_Pin1_4 | 239 | 244 | PF00397 | 0.635 |
DOC_WW_Pin1_4 | 249 | 254 | PF00397 | 0.545 |
LIG_14-3-3_CanoR_1 | 165 | 171 | PF00244 | 0.411 |
LIG_14-3-3_CanoR_1 | 283 | 290 | PF00244 | 0.555 |
LIG_14-3-3_CanoR_1 | 295 | 300 | PF00244 | 0.425 |
LIG_14-3-3_CanoR_1 | 51 | 61 | PF00244 | 0.280 |
LIG_Actin_WH2_2 | 400 | 417 | PF00022 | 0.545 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.679 |
LIG_BIR_III_1 | 1 | 5 | PF00653 | 0.631 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.631 |
LIG_Clathr_ClatBox_1 | 396 | 400 | PF01394 | 0.447 |
LIG_FHA_1 | 166 | 172 | PF00498 | 0.394 |
LIG_FHA_1 | 283 | 289 | PF00498 | 0.509 |
LIG_FHA_1 | 70 | 76 | PF00498 | 0.315 |
LIG_FHA_2 | 12 | 18 | PF00498 | 0.556 |
LIG_FHA_2 | 153 | 159 | PF00498 | 0.391 |
LIG_FHA_2 | 369 | 375 | PF00498 | 0.560 |
LIG_LIR_Gen_1 | 155 | 164 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 155 | 160 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 200 | 206 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 208 | 213 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 99 | 105 | PF02991 | 0.386 |
LIG_LYPXL_yS_3 | 210 | 213 | PF13949 | 0.483 |
LIG_NRBOX | 100 | 106 | PF00104 | 0.326 |
LIG_NRBOX | 179 | 185 | PF00104 | 0.432 |
LIG_PDZ_Class_2 | 414 | 419 | PF00595 | 0.568 |
LIG_Pex14_1 | 203 | 207 | PF04695 | 0.492 |
LIG_Pex14_2 | 50 | 54 | PF04695 | 0.312 |
LIG_REV1ctd_RIR_1 | 47 | 55 | PF16727 | 0.312 |
LIG_SH2_CRK | 157 | 161 | PF00017 | 0.457 |
LIG_SH2_SRC | 137 | 140 | PF00017 | 0.326 |
LIG_SH2_STAP1 | 128 | 132 | PF00017 | 0.377 |
LIG_SH2_STAP1 | 166 | 170 | PF00017 | 0.399 |
LIG_SH2_STAT5 | 330 | 333 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 337 | 340 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 37 | 40 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 53 | 56 | PF00017 | 0.312 |
MOD_CDC14_SPxK_1 | 244 | 247 | PF00782 | 0.586 |
MOD_CDC14_SPxK_1 | 252 | 255 | PF00782 | 0.577 |
MOD_CDK_SPxK_1 | 241 | 247 | PF00069 | 0.595 |
MOD_CDK_SPxK_1 | 249 | 255 | PF00069 | 0.567 |
MOD_CDK_SPxxK_3 | 241 | 248 | PF00069 | 0.632 |
MOD_CK1_1 | 221 | 227 | PF00069 | 0.503 |
MOD_CK1_1 | 233 | 239 | PF00069 | 0.531 |
MOD_CK1_1 | 262 | 268 | PF00069 | 0.632 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.329 |
MOD_CK2_1 | 368 | 374 | PF00069 | 0.559 |
MOD_GlcNHglycan | 143 | 146 | PF01048 | 0.454 |
MOD_GlcNHglycan | 193 | 196 | PF01048 | 0.498 |
MOD_GlcNHglycan | 220 | 223 | PF01048 | 0.509 |
MOD_GlcNHglycan | 227 | 230 | PF01048 | 0.505 |
MOD_GlcNHglycan | 232 | 236 | PF01048 | 0.499 |
MOD_GlcNHglycan | 262 | 265 | PF01048 | 0.648 |
MOD_GlcNHglycan | 269 | 272 | PF01048 | 0.591 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.547 |
MOD_GlcNHglycan | 364 | 367 | PF01048 | 0.567 |
MOD_GlcNHglycan | 382 | 385 | PF01048 | 0.369 |
MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.388 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.306 |
MOD_GlcNHglycan | 82 | 85 | PF01048 | 0.278 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.297 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.570 |
MOD_GSK3_1 | 256 | 263 | PF00069 | 0.643 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.468 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.578 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.378 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.291 |
MOD_LATS_1 | 139 | 145 | PF00433 | 0.426 |
MOD_LATS_1 | 78 | 84 | PF00433 | 0.378 |
MOD_NEK2_1 | 190 | 195 | PF00069 | 0.463 |
MOD_NEK2_1 | 306 | 311 | PF00069 | 0.554 |
MOD_NEK2_1 | 313 | 318 | PF00069 | 0.506 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.321 |
MOD_NEK2_1 | 90 | 95 | PF00069 | 0.312 |
MOD_NEK2_2 | 123 | 128 | PF00069 | 0.415 |
MOD_NEK2_2 | 368 | 373 | PF00069 | 0.461 |
MOD_PKA_2 | 191 | 197 | PF00069 | 0.411 |
MOD_PKA_2 | 282 | 288 | PF00069 | 0.556 |
MOD_PKA_2 | 306 | 312 | PF00069 | 0.539 |
MOD_PKA_2 | 380 | 386 | PF00069 | 0.496 |
MOD_PKB_1 | 295 | 303 | PF00069 | 0.545 |
MOD_Plk_1 | 301 | 307 | PF00069 | 0.475 |
MOD_Plk_1 | 4 | 10 | PF00069 | 0.635 |
MOD_Plk_2-3 | 13 | 19 | PF00069 | 0.555 |
MOD_Plk_4 | 123 | 129 | PF00069 | 0.339 |
MOD_Plk_4 | 152 | 158 | PF00069 | 0.378 |
MOD_Plk_4 | 166 | 172 | PF00069 | 0.390 |
MOD_Plk_4 | 262 | 268 | PF00069 | 0.605 |
MOD_Plk_4 | 70 | 76 | PF00069 | 0.312 |
MOD_ProDKin_1 | 239 | 245 | PF00069 | 0.632 |
MOD_ProDKin_1 | 249 | 255 | PF00069 | 0.547 |
MOD_SUMO_for_1 | 132 | 135 | PF00179 | 0.373 |
MOD_SUMO_rev_2 | 383 | 392 | PF00179 | 0.542 |
TRG_ENDOCYTIC_2 | 157 | 160 | PF00928 | 0.447 |
TRG_ENDOCYTIC_2 | 188 | 191 | PF00928 | 0.429 |
TRG_ENDOCYTIC_2 | 210 | 213 | PF00928 | 0.483 |
TRG_ER_diArg_1 | 201 | 203 | PF00400 | 0.432 |
TRG_ER_diArg_1 | 204 | 206 | PF00400 | 0.427 |
TRG_ER_diArg_1 | 246 | 248 | PF00400 | 0.665 |
TRG_ER_diArg_1 | 294 | 297 | PF00400 | 0.470 |
TRG_Pf-PMV_PEXEL_1 | 204 | 208 | PF00026 | 0.428 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZP2 | Leptomonas seymouri | 46% | 99% |
A4H9Q7 | Leishmania braziliensis | 68% | 99% |
A4HY26 | Leishmania infantum | 100% | 100% |
E9ART9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
Q4QDN4 | Leishmania major | 91% | 100% |