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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 1, no: 10 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: A4H3R2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 142 | 146 | PF00656 | 0.318 |
CLV_C14_Caspase3-7 | 86 | 90 | PF00656 | 0.404 |
CLV_MEL_PAP_1 | 192 | 198 | PF00089 | 0.540 |
CLV_NRD_NRD_1 | 122 | 124 | PF00675 | 0.413 |
CLV_NRD_NRD_1 | 150 | 152 | PF00675 | 0.509 |
CLV_NRD_NRD_1 | 194 | 196 | PF00675 | 0.511 |
CLV_NRD_NRD_1 | 363 | 365 | PF00675 | 0.346 |
CLV_PCSK_KEX2_1 | 122 | 124 | PF00082 | 0.393 |
CLV_PCSK_KEX2_1 | 150 | 152 | PF00082 | 0.374 |
CLV_PCSK_KEX2_1 | 194 | 196 | PF00082 | 0.511 |
CLV_PCSK_KEX2_1 | 240 | 242 | PF00082 | 0.502 |
CLV_PCSK_PC1ET2_1 | 240 | 242 | PF00082 | 0.418 |
CLV_Separin_Metazoa | 147 | 151 | PF03568 | 0.302 |
DEG_APCC_DBOX_1 | 149 | 157 | PF00400 | 0.327 |
DEG_SPOP_SBC_1 | 107 | 111 | PF00917 | 0.241 |
DEG_SPOP_SBC_1 | 225 | 229 | PF00917 | 0.421 |
DEG_SPOP_SBC_1 | 31 | 35 | PF00917 | 0.722 |
DOC_PP1_RVXF_1 | 97 | 104 | PF00149 | 0.381 |
DOC_PP2B_LxvP_1 | 27 | 30 | PF13499 | 0.423 |
DOC_PP4_FxxP_1 | 37 | 40 | PF00568 | 0.494 |
DOC_USP7_MATH_1 | 219 | 223 | PF00917 | 0.629 |
DOC_USP7_MATH_1 | 249 | 253 | PF00917 | 0.424 |
DOC_USP7_MATH_1 | 31 | 35 | PF00917 | 0.510 |
DOC_USP7_MATH_1 | 47 | 51 | PF00917 | 0.508 |
DOC_USP7_MATH_2 | 59 | 65 | PF00917 | 0.285 |
DOC_WW_Pin1_4 | 18 | 23 | PF00397 | 0.618 |
DOC_WW_Pin1_4 | 92 | 97 | PF00397 | 0.498 |
LIG_14-3-3_CanoR_1 | 127 | 135 | PF00244 | 0.460 |
LIG_14-3-3_CanoR_1 | 151 | 157 | PF00244 | 0.431 |
LIG_14-3-3_CanoR_1 | 207 | 211 | PF00244 | 0.390 |
LIG_14-3-3_CanoR_1 | 296 | 302 | PF00244 | 0.463 |
LIG_14-3-3_CanoR_1 | 9 | 16 | PF00244 | 0.558 |
LIG_Actin_WH2_2 | 109 | 124 | PF00022 | 0.421 |
LIG_BIR_III_4 | 46 | 50 | PF00653 | 0.275 |
LIG_BRCT_BRCA1_1 | 33 | 37 | PF00533 | 0.510 |
LIG_BRCT_BRCA1_1 | 63 | 67 | PF00533 | 0.282 |
LIG_deltaCOP1_diTrp_1 | 57 | 67 | PF00928 | 0.339 |
LIG_FHA_1 | 107 | 113 | PF00498 | 0.381 |
LIG_FHA_1 | 308 | 314 | PF00498 | 0.348 |
LIG_FHA_1 | 326 | 332 | PF00498 | 0.438 |
LIG_FHA_1 | 73 | 79 | PF00498 | 0.493 |
LIG_FHA_2 | 109 | 115 | PF00498 | 0.400 |
LIG_FHA_2 | 128 | 134 | PF00498 | 0.334 |
LIG_FHA_2 | 140 | 146 | PF00498 | 0.476 |
LIG_LIR_Apic_2 | 34 | 40 | PF02991 | 0.502 |
LIG_LIR_Gen_1 | 110 | 121 | PF02991 | 0.410 |
LIG_LIR_Gen_1 | 126 | 136 | PF02991 | 0.292 |
LIG_LIR_Gen_1 | 229 | 236 | PF02991 | 0.485 |
LIG_LIR_Gen_1 | 270 | 281 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 110 | 116 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 126 | 132 | PF02991 | 0.278 |
LIG_LIR_Nem_3 | 229 | 235 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 270 | 276 | PF02991 | 0.361 |
LIG_MYND_1 | 347 | 351 | PF01753 | 0.504 |
LIG_Pex14_1 | 125 | 129 | PF04695 | 0.357 |
LIG_SH2_CRK | 232 | 236 | PF00017 | 0.370 |
LIG_SH2_CRK | 367 | 371 | PF00017 | 0.423 |
LIG_SH2_NCK_1 | 232 | 236 | PF00017 | 0.353 |
LIG_SH2_SRC | 210 | 213 | PF00017 | 0.226 |
LIG_SH2_SRC | 232 | 235 | PF00017 | 0.349 |
LIG_SH2_SRC | 87 | 90 | PF00017 | 0.561 |
LIG_SH2_STAP1 | 210 | 214 | PF00017 | 0.363 |
LIG_SH2_STAP1 | 232 | 236 | PF00017 | 0.339 |
LIG_SH2_STAP1 | 25 | 29 | PF00017 | 0.582 |
LIG_SH2_STAP1 | 367 | 371 | PF00017 | 0.358 |
LIG_SH2_STAT5 | 115 | 118 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 129 | 132 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 87 | 90 | PF00017 | 0.322 |
LIG_SH3_3 | 102 | 108 | PF00018 | 0.304 |
LIG_SH3_3 | 274 | 280 | PF00018 | 0.334 |
LIG_SH3_3 | 341 | 347 | PF00018 | 0.378 |
LIG_Sin3_3 | 12 | 19 | PF02671 | 0.449 |
LIG_SUMO_SIM_anti_2 | 334 | 340 | PF11976 | 0.315 |
LIG_SUMO_SIM_par_1 | 303 | 310 | PF11976 | 0.404 |
LIG_SUMO_SIM_par_1 | 333 | 340 | PF11976 | 0.335 |
LIG_TRAF2_1 | 242 | 245 | PF00917 | 0.278 |
LIG_TRAF2_1 | 265 | 268 | PF00917 | 0.521 |
LIG_UBA3_1 | 358 | 365 | PF00899 | 0.433 |
MOD_CDK_SPxxK_3 | 92 | 99 | PF00069 | 0.548 |
MOD_CK1_1 | 322 | 328 | PF00069 | 0.423 |
MOD_CK2_1 | 108 | 114 | PF00069 | 0.543 |
MOD_CK2_1 | 127 | 133 | PF00069 | 0.266 |
MOD_CK2_1 | 210 | 216 | PF00069 | 0.377 |
MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.510 |
MOD_GlcNHglycan | 220 | 224 | PF01048 | 0.545 |
MOD_GlcNHglycan | 236 | 239 | PF01048 | 0.352 |
MOD_GlcNHglycan | 244 | 249 | PF01048 | 0.454 |
MOD_GlcNHglycan | 339 | 342 | PF01048 | 0.374 |
MOD_GlcNHglycan | 376 | 381 | PF01048 | 0.580 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.269 |
MOD_GSK3_1 | 317 | 324 | PF00069 | 0.553 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.494 |
MOD_GSK3_1 | 376 | 383 | PF00069 | 0.540 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.482 |
MOD_N-GLC_1 | 117 | 122 | PF02516 | 0.494 |
MOD_N-GLC_1 | 127 | 132 | PF02516 | 0.410 |
MOD_N-GLC_1 | 73 | 78 | PF02516 | 0.514 |
MOD_NEK2_1 | 214 | 219 | PF00069 | 0.545 |
MOD_NEK2_1 | 236 | 241 | PF00069 | 0.487 |
MOD_NEK2_1 | 32 | 37 | PF00069 | 0.653 |
MOD_NEK2_1 | 336 | 341 | PF00069 | 0.327 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.586 |
MOD_NEK2_2 | 108 | 113 | PF00069 | 0.372 |
MOD_NEK2_2 | 210 | 215 | PF00069 | 0.242 |
MOD_NEK2_2 | 47 | 52 | PF00069 | 0.436 |
MOD_PIKK_1 | 20 | 26 | PF00454 | 0.507 |
MOD_PIKK_1 | 317 | 323 | PF00454 | 0.463 |
MOD_PIKK_1 | 73 | 79 | PF00454 | 0.285 |
MOD_PKA_1 | 158 | 164 | PF00069 | 0.300 |
MOD_PKA_2 | 206 | 212 | PF00069 | 0.311 |
MOD_PKA_2 | 214 | 220 | PF00069 | 0.437 |
MOD_PKA_2 | 307 | 313 | PF00069 | 0.367 |
MOD_PKA_2 | 322 | 328 | PF00069 | 0.460 |
MOD_PKA_2 | 8 | 14 | PF00069 | 0.621 |
MOD_Plk_1 | 117 | 123 | PF00069 | 0.469 |
MOD_Plk_1 | 127 | 133 | PF00069 | 0.439 |
MOD_Plk_1 | 166 | 172 | PF00069 | 0.295 |
MOD_Plk_1 | 73 | 79 | PF00069 | 0.513 |
MOD_Plk_2-3 | 41 | 47 | PF00069 | 0.428 |
MOD_Plk_2-3 | 61 | 67 | PF00069 | 0.436 |
MOD_Plk_4 | 108 | 114 | PF00069 | 0.539 |
MOD_Plk_4 | 166 | 172 | PF00069 | 0.524 |
MOD_Plk_4 | 188 | 194 | PF00069 | 0.299 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.671 |
MOD_Plk_4 | 300 | 306 | PF00069 | 0.353 |
MOD_Plk_4 | 32 | 38 | PF00069 | 0.638 |
MOD_Plk_4 | 331 | 337 | PF00069 | 0.340 |
MOD_Plk_4 | 354 | 360 | PF00069 | 0.411 |
MOD_ProDKin_1 | 18 | 24 | PF00069 | 0.618 |
MOD_ProDKin_1 | 92 | 98 | PF00069 | 0.495 |
TRG_DiLeu_BaLyEn_6 | 345 | 350 | PF01217 | 0.343 |
TRG_ENDOCYTIC_2 | 113 | 116 | PF00928 | 0.429 |
TRG_ENDOCYTIC_2 | 129 | 132 | PF00928 | 0.265 |
TRG_ENDOCYTIC_2 | 205 | 208 | PF00928 | 0.348 |
TRG_ENDOCYTIC_2 | 232 | 235 | PF00928 | 0.367 |
TRG_ENDOCYTIC_2 | 367 | 370 | PF00928 | 0.365 |
TRG_ER_diArg_1 | 121 | 123 | PF00400 | 0.419 |
TRG_ER_diArg_1 | 149 | 151 | PF00400 | 0.465 |
TRG_ER_diArg_1 | 193 | 195 | PF00400 | 0.545 |
TRG_ER_diArg_1 | 81 | 84 | PF00400 | 0.360 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IG75 | Leptomonas seymouri | 52% | 100% |
A0A0S4J6P5 | Bodo saltans | 25% | 90% |
A0A1X0PAK7 | Trypanosomatidae | 37% | 99% |
A0A3S5H7M1 | Leishmania donovani | 69% | 100% |
A0A422NJ09 | Trypanosoma rangeli | 37% | 100% |
A4I4Y1 | Leishmania infantum | 69% | 100% |
C9ZLM3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
E9AEE9 | Leishmania major | 70% | 100% |
E9ALD7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 66% | 100% |
V5B889 | Trypanosoma cruzi | 39% | 93% |