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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: E9ANS5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 274 | 278 | PF00656 | 0.377 |
CLV_C14_Caspase3-7 | 34 | 38 | PF00656 | 0.306 |
CLV_MEL_PAP_1 | 80 | 86 | PF00089 | 0.438 |
CLV_NRD_NRD_1 | 352 | 354 | PF00675 | 0.417 |
CLV_PCSK_KEX2_1 | 242 | 244 | PF00082 | 0.557 |
CLV_PCSK_KEX2_1 | 341 | 343 | PF00082 | 0.475 |
CLV_PCSK_PC1ET2_1 | 242 | 244 | PF00082 | 0.442 |
CLV_PCSK_PC1ET2_1 | 341 | 343 | PF00082 | 0.453 |
CLV_PCSK_SKI1_1 | 192 | 196 | PF00082 | 0.474 |
CLV_PCSK_SKI1_1 | 338 | 342 | PF00082 | 0.396 |
CLV_PCSK_SKI1_1 | 51 | 55 | PF00082 | 0.360 |
CLV_PCSK_SKI1_1 | 76 | 80 | PF00082 | 0.517 |
DEG_APCC_DBOX_1 | 230 | 238 | PF00400 | 0.590 |
DEG_APCC_DBOX_1 | 310 | 318 | PF00400 | 0.292 |
DOC_MAPK_gen_1 | 341 | 349 | PF00069 | 0.537 |
DOC_MAPK_MEF2A_6 | 342 | 351 | PF00069 | 0.500 |
DOC_PP1_RVXF_1 | 270 | 276 | PF00149 | 0.550 |
DOC_PP4_FxxP_1 | 64 | 67 | PF00568 | 0.522 |
DOC_SPAK_OSR1_1 | 83 | 87 | PF12202 | 0.471 |
DOC_USP7_MATH_1 | 217 | 221 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 229 | 233 | PF00917 | 0.509 |
DOC_USP7_MATH_1 | 263 | 267 | PF00917 | 0.605 |
DOC_USP7_MATH_1 | 36 | 40 | PF00917 | 0.410 |
DOC_USP7_UBL2_3 | 238 | 242 | PF12436 | 0.545 |
DOC_WW_Pin1_4 | 106 | 111 | PF00397 | 0.626 |
LIG_14-3-3_CanoR_1 | 177 | 182 | PF00244 | 0.361 |
LIG_14-3-3_CanoR_1 | 231 | 235 | PF00244 | 0.386 |
LIG_14-3-3_CanoR_1 | 264 | 270 | PF00244 | 0.487 |
LIG_BIR_III_4 | 37 | 41 | PF00653 | 0.306 |
LIG_CaM_IQ_9 | 314 | 329 | PF13499 | 0.293 |
LIG_DLG_GKlike_1 | 177 | 185 | PF00625 | 0.291 |
LIG_DLG_GKlike_1 | 353 | 360 | PF00625 | 0.383 |
LIG_FHA_1 | 191 | 197 | PF00498 | 0.405 |
LIG_FHA_1 | 55 | 61 | PF00498 | 0.410 |
LIG_FHA_2 | 117 | 123 | PF00498 | 0.601 |
LIG_FHA_2 | 269 | 275 | PF00498 | 0.372 |
LIG_LIR_Apic_2 | 14 | 18 | PF02991 | 0.383 |
LIG_LIR_Apic_2 | 56 | 61 | PF02991 | 0.373 |
LIG_LIR_Gen_1 | 176 | 185 | PF02991 | 0.338 |
LIG_LIR_Gen_1 | 208 | 218 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 176 | 181 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 20 | 25 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 203 | 207 | PF02991 | 0.575 |
LIG_LIR_Nem_3 | 208 | 213 | PF02991 | 0.584 |
LIG_LIR_Nem_3 | 335 | 340 | PF02991 | 0.547 |
LIG_MYND_3 | 94 | 98 | PF01753 | 0.518 |
LIG_Pex14_1 | 206 | 210 | PF04695 | 0.541 |
LIG_SH2_CRK | 15 | 19 | PF00017 | 0.355 |
LIG_SH2_CRK | 58 | 62 | PF00017 | 0.514 |
LIG_SH2_NCK_1 | 15 | 19 | PF00017 | 0.410 |
LIG_SH2_NCK_1 | 58 | 62 | PF00017 | 0.514 |
LIG_SH2_PTP2 | 62 | 65 | PF00017 | 0.559 |
LIG_SH2_SRC | 10 | 13 | PF00017 | 0.351 |
LIG_SH2_SRC | 15 | 18 | PF00017 | 0.317 |
LIG_SH2_STAT5 | 298 | 301 | PF00017 | 0.400 |
LIG_SH2_STAT5 | 58 | 61 | PF00017 | 0.472 |
LIG_SH2_STAT5 | 62 | 65 | PF00017 | 0.531 |
LIG_SH3_3 | 107 | 113 | PF00018 | 0.647 |
LIG_SH3_3 | 213 | 219 | PF00018 | 0.369 |
LIG_SH3_3 | 60 | 66 | PF00018 | 0.447 |
LIG_TRAF2_1 | 256 | 259 | PF00917 | 0.490 |
LIG_WRC_WIRS_1 | 201 | 206 | PF05994 | 0.410 |
MOD_CK1_1 | 184 | 190 | PF00069 | 0.349 |
MOD_CK1_1 | 220 | 226 | PF00069 | 0.643 |
MOD_CK1_1 | 268 | 274 | PF00069 | 0.481 |
MOD_CK1_1 | 56 | 62 | PF00069 | 0.435 |
MOD_GlcNHglycan | 19 | 22 | PF01048 | 0.306 |
MOD_GlcNHglycan | 37 | 41 | PF01048 | 0.193 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.554 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.440 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.485 |
MOD_GSK3_1 | 264 | 271 | PF00069 | 0.314 |
MOD_N-GLC_1 | 211 | 216 | PF02516 | 0.363 |
MOD_NEK2_1 | 181 | 186 | PF00069 | 0.549 |
MOD_NEK2_1 | 251 | 256 | PF00069 | 0.490 |
MOD_PIKK_1 | 137 | 143 | PF00454 | 0.472 |
MOD_PKA_1 | 353 | 359 | PF00069 | 0.410 |
MOD_PKA_2 | 230 | 236 | PF00069 | 0.584 |
MOD_PKA_2 | 249 | 255 | PF00069 | 0.591 |
MOD_PKA_2 | 263 | 269 | PF00069 | 0.400 |
MOD_PKB_1 | 175 | 183 | PF00069 | 0.446 |
MOD_Plk_1 | 181 | 187 | PF00069 | 0.562 |
MOD_Plk_1 | 211 | 217 | PF00069 | 0.623 |
MOD_Plk_1 | 246 | 252 | PF00069 | 0.487 |
MOD_Plk_4 | 211 | 217 | PF00069 | 0.557 |
MOD_ProDKin_1 | 106 | 112 | PF00069 | 0.618 |
MOD_SUMO_for_1 | 301 | 304 | PF00179 | 0.361 |
MOD_SUMO_rev_2 | 232 | 240 | PF00179 | 0.535 |
TRG_DiLeu_BaEn_4 | 246 | 252 | PF01217 | 0.493 |
TRG_DiLeu_BaLyEn_6 | 121 | 126 | PF01217 | 0.603 |
TRG_DiLeu_BaLyEn_6 | 73 | 78 | PF01217 | 0.487 |
TRG_DiLeu_BaLyEn_6 | 92 | 97 | PF01217 | 0.550 |
TRG_ENDOCYTIC_2 | 207 | 210 | PF00928 | 0.578 |
TRG_ENDOCYTIC_2 | 337 | 340 | PF00928 | 0.503 |
TRG_ER_diArg_1 | 132 | 135 | PF00400 | 0.534 |
TRG_ER_diArg_1 | 319 | 322 | PF00400 | 0.446 |
TRG_ER_diArg_1 | 377 | 380 | PF00400 | 0.625 |
TRG_Pf-PMV_PEXEL_1 | 124 | 129 | PF00026 | 0.491 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IJ47 | Leptomonas seymouri | 47% | 100% |
A0A1X0NUT5 | Trypanosomatidae | 25% | 100% |
A0A3Q8I836 | Leishmania donovani | 81% | 100% |
A0A3R7RDU1 | Trypanosoma rangeli | 29% | 98% |
A4H6R1 | Leishmania braziliensis | 67% | 100% |
A4HV44 | Leishmania infantum | 80% | 100% |
D0A7A4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 100% |
Q4QGU4 | Leishmania major | 83% | 100% |
V5DT68 | Trypanosoma cruzi | 30% | 98% |