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: 17 |
NetGPI | no | yes: 0, no: 17 |
Related structures:
AlphaFold database: E9AVU5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 148 | 150 | PF00675 | 0.491 |
CLV_NRD_NRD_1 | 351 | 353 | PF00675 | 0.418 |
CLV_NRD_NRD_1 | 44 | 46 | PF00675 | 0.346 |
CLV_NRD_NRD_1 | 5 | 7 | PF00675 | 0.554 |
CLV_PCSK_KEX2_1 | 148 | 150 | PF00082 | 0.491 |
CLV_PCSK_KEX2_1 | 351 | 353 | PF00082 | 0.480 |
CLV_PCSK_KEX2_1 | 44 | 46 | PF00082 | 0.346 |
CLV_PCSK_KEX2_1 | 5 | 7 | PF00082 | 0.554 |
CLV_PCSK_SKI1_1 | 406 | 410 | PF00082 | 0.485 |
DEG_APCC_DBOX_1 | 5 | 13 | PF00400 | 0.346 |
DEG_ODPH_VHL_1 | 84 | 97 | PF01847 | 0.463 |
DEG_SPOP_SBC_1 | 126 | 130 | PF00917 | 0.417 |
DEG_SPOP_SBC_1 | 198 | 202 | PF00917 | 0.519 |
DOC_CDC14_PxL_1 | 153 | 161 | PF14671 | 0.359 |
DOC_MAPK_gen_1 | 219 | 228 | PF00069 | 0.459 |
DOC_MAPK_gen_1 | 379 | 388 | PF00069 | 0.518 |
DOC_MAPK_gen_1 | 44 | 52 | PF00069 | 0.339 |
DOC_MAPK_gen_1 | 5 | 11 | PF00069 | 0.484 |
DOC_MAPK_gen_1 | 74 | 83 | PF00069 | 0.397 |
DOC_MAPK_HePTP_8 | 378 | 390 | PF00069 | 0.405 |
DOC_MAPK_MEF2A_6 | 219 | 228 | PF00069 | 0.553 |
DOC_MAPK_MEF2A_6 | 316 | 324 | PF00069 | 0.293 |
DOC_MAPK_MEF2A_6 | 381 | 390 | PF00069 | 0.555 |
DOC_MAPK_MEF2A_6 | 44 | 52 | PF00069 | 0.383 |
DOC_PP1_RVXF_1 | 403 | 410 | PF00149 | 0.370 |
DOC_PP1_RVXF_1 | 6 | 12 | PF00149 | 0.335 |
DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.429 |
DOC_USP7_MATH_1 | 185 | 189 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 198 | 202 | PF00917 | 0.560 |
DOC_USP7_MATH_1 | 233 | 237 | PF00917 | 0.635 |
DOC_USP7_MATH_1 | 275 | 279 | PF00917 | 0.471 |
DOC_USP7_MATH_1 | 304 | 308 | PF00917 | 0.487 |
DOC_USP7_MATH_1 | 331 | 335 | PF00917 | 0.521 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.598 |
DOC_USP7_MATH_1 | 391 | 395 | PF00917 | 0.561 |
DOC_WW_Pin1_4 | 163 | 168 | PF00397 | 0.561 |
DOC_WW_Pin1_4 | 229 | 234 | PF00397 | 0.555 |
LIG_14-3-3_CanoR_1 | 199 | 207 | PF00244 | 0.571 |
LIG_14-3-3_CanoR_1 | 351 | 355 | PF00244 | 0.443 |
LIG_14-3-3_CanoR_1 | 45 | 51 | PF00244 | 0.409 |
LIG_14-3-3_CanoR_1 | 6 | 12 | PF00244 | 0.403 |
LIG_BRCT_BRCA1_1 | 306 | 310 | PF00533 | 0.480 |
LIG_BRCT_BRCA1_1 | 52 | 56 | PF00533 | 0.358 |
LIG_Clathr_ClatBox_1 | 314 | 318 | PF01394 | 0.363 |
LIG_eIF4E_1 | 91 | 97 | PF01652 | 0.395 |
LIG_FHA_1 | 351 | 357 | PF00498 | 0.309 |
LIG_FHA_2 | 207 | 213 | PF00498 | 0.426 |
LIG_IRF3_LxIS_1 | 48 | 53 | PF10401 | 0.416 |
LIG_LIR_Gen_1 | 64 | 70 | PF02991 | 0.424 |
LIG_LIR_Gen_1 | 78 | 87 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 249 | 255 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 64 | 68 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 78 | 83 | PF02991 | 0.368 |
LIG_Pex14_2 | 355 | 359 | PF04695 | 0.450 |
LIG_SH2_CRK | 253 | 257 | PF00017 | 0.360 |
LIG_SH2_CRK | 80 | 84 | PF00017 | 0.465 |
LIG_SH2_SRC | 91 | 94 | PF00017 | 0.400 |
LIG_SH2_STAP1 | 122 | 126 | PF00017 | 0.404 |
LIG_SH2_STAT3 | 420 | 423 | PF00017 | 0.496 |
LIG_SH2_STAT5 | 122 | 125 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 263 | 266 | PF00017 | 0.425 |
LIG_SH2_STAT5 | 296 | 299 | PF00017 | 0.353 |
LIG_SH2_STAT5 | 336 | 339 | PF00017 | 0.393 |
LIG_SH2_STAT5 | 354 | 357 | PF00017 | 0.252 |
LIG_SH2_STAT5 | 91 | 94 | PF00017 | 0.414 |
LIG_SH3_2 | 39 | 44 | PF14604 | 0.450 |
LIG_SH3_3 | 151 | 157 | PF00018 | 0.234 |
LIG_SH3_3 | 224 | 230 | PF00018 | 0.463 |
LIG_SH3_3 | 36 | 42 | PF00018 | 0.495 |
LIG_SH3_3 | 385 | 391 | PF00018 | 0.451 |
LIG_SH3_3 | 80 | 86 | PF00018 | 0.473 |
LIG_SUMO_SIM_anti_2 | 318 | 323 | PF11976 | 0.296 |
LIG_SUMO_SIM_par_1 | 318 | 323 | PF11976 | 0.296 |
LIG_UBA3_1 | 213 | 220 | PF00899 | 0.489 |
LIG_WRC_WIRS_1 | 150 | 155 | PF05994 | 0.471 |
MOD_CDK_SPK_2 | 234 | 239 | PF00069 | 0.647 |
MOD_CK1_1 | 125 | 131 | PF00069 | 0.642 |
MOD_CK1_1 | 200 | 206 | PF00069 | 0.521 |
MOD_CK1_1 | 298 | 304 | PF00069 | 0.355 |
MOD_CK2_1 | 199 | 205 | PF00069 | 0.663 |
MOD_CK2_1 | 58 | 64 | PF00069 | 0.486 |
MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.547 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.713 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.413 |
MOD_GlcNHglycan | 187 | 190 | PF01048 | 0.546 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.592 |
MOD_GlcNHglycan | 331 | 334 | PF01048 | 0.549 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.564 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.545 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.475 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.535 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.602 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.632 |
MOD_GSK3_1 | 229 | 236 | PF00069 | 0.705 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.710 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.431 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.377 |
MOD_GSK3_1 | 54 | 61 | PF00069 | 0.437 |
MOD_GSK3_1 | 7 | 14 | PF00069 | 0.311 |
MOD_N-GLC_1 | 46 | 51 | PF02516 | 0.393 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.394 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.397 |
MOD_NEK2_1 | 95 | 100 | PF00069 | 0.446 |
MOD_NEK2_2 | 72 | 77 | PF00069 | 0.366 |
MOD_PIKK_1 | 120 | 126 | PF00454 | 0.324 |
MOD_PIKK_1 | 275 | 281 | PF00454 | 0.593 |
MOD_PKA_2 | 120 | 126 | PF00069 | 0.398 |
MOD_PKA_2 | 198 | 204 | PF00069 | 0.641 |
MOD_PKA_2 | 271 | 277 | PF00069 | 0.474 |
MOD_PKA_2 | 350 | 356 | PF00069 | 0.438 |
MOD_PKA_2 | 7 | 13 | PF00069 | 0.395 |
MOD_Plk_1 | 298 | 304 | PF00069 | 0.419 |
MOD_Plk_1 | 46 | 52 | PF00069 | 0.388 |
MOD_Plk_4 | 149 | 155 | PF00069 | 0.439 |
MOD_Plk_4 | 206 | 212 | PF00069 | 0.504 |
MOD_Plk_4 | 46 | 52 | PF00069 | 0.321 |
MOD_Plk_4 | 7 | 13 | PF00069 | 0.390 |
MOD_ProDKin_1 | 163 | 169 | PF00069 | 0.555 |
MOD_ProDKin_1 | 229 | 235 | PF00069 | 0.563 |
MOD_SUMO_rev_2 | 212 | 221 | PF00179 | 0.440 |
MOD_SUMO_rev_2 | 400 | 408 | PF00179 | 0.401 |
MOD_SUMO_rev_2 | 53 | 61 | PF00179 | 0.356 |
TRG_ENDOCYTIC_2 | 263 | 266 | PF00928 | 0.367 |
TRG_ENDOCYTIC_2 | 80 | 83 | PF00928 | 0.400 |
TRG_ER_diArg_1 | 147 | 149 | PF00400 | 0.499 |
TRG_ER_diArg_1 | 350 | 352 | PF00400 | 0.423 |
TRG_ER_diArg_1 | 4 | 6 | PF00400 | 0.537 |
TRG_NES_CRM1_1 | 205 | 218 | PF08389 | 0.394 |
TRG_NES_CRM1_1 | 312 | 323 | PF08389 | 0.369 |
TRG_Pf-PMV_PEXEL_1 | 373 | 377 | PF00026 | 0.531 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I0M2 | Leptomonas seymouri | 37% | 94% |
A0A0N1PFX0 | Leptomonas seymouri | 59% | 94% |
A0A0S4J8Q0 | Bodo saltans | 36% | 100% |
A0A1X0NTE2 | Trypanosomatidae | 41% | 100% |
A0A3Q8IFK3 | Leishmania donovani | 47% | 92% |
A0A3S7WXD8 | Leishmania donovani | 91% | 100% |
A0A422NHR8 | Trypanosoma rangeli | 40% | 100% |
A4HCF4 | Leishmania braziliensis | 40% | 100% |
A4HZY3 | Leishmania infantum | 47% | 92% |
A4HZY4 | Leishmania infantum | 91% | 100% |
C9ZSM3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
C9ZVB8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 23% | 100% |
E9AVU4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 44% | 100% |
Q4QBN4 | Leishmania major | 90% | 99% |
Q4QBN5 | Leishmania major | 42% | 100% |
V5BVW3 | Trypanosoma cruzi | 40% | 100% |