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: E9AQG3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 361 | 365 | PF00656 | 0.536 |
CLV_NRD_NRD_1 | 286 | 288 | PF00675 | 0.414 |
CLV_NRD_NRD_1 | 372 | 374 | PF00675 | 0.588 |
CLV_NRD_NRD_1 | 41 | 43 | PF00675 | 0.466 |
CLV_NRD_NRD_1 | 76 | 78 | PF00675 | 0.622 |
CLV_PCSK_KEX2_1 | 187 | 189 | PF00082 | 0.483 |
CLV_PCSK_KEX2_1 | 323 | 325 | PF00082 | 0.517 |
CLV_PCSK_KEX2_1 | 372 | 374 | PF00082 | 0.588 |
CLV_PCSK_KEX2_1 | 41 | 43 | PF00082 | 0.466 |
CLV_PCSK_KEX2_1 | 75 | 77 | PF00082 | 0.623 |
CLV_PCSK_KEX2_1 | 89 | 91 | PF00082 | 0.609 |
CLV_PCSK_PC1ET2_1 | 187 | 189 | PF00082 | 0.447 |
CLV_PCSK_PC1ET2_1 | 323 | 325 | PF00082 | 0.517 |
CLV_PCSK_PC1ET2_1 | 89 | 91 | PF00082 | 0.609 |
CLV_PCSK_PC7_1 | 85 | 91 | PF00082 | 0.677 |
CLV_PCSK_SKI1_1 | 263 | 267 | PF00082 | 0.490 |
CLV_PCSK_SKI1_1 | 295 | 299 | PF00082 | 0.501 |
CLV_PCSK_SKI1_1 | 77 | 81 | PF00082 | 0.706 |
CLV_Separin_Metazoa | 222 | 226 | PF03568 | 0.385 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.662 |
DEG_SPOP_SBC_1 | 10 | 14 | PF00917 | 0.528 |
DEG_SPOP_SBC_1 | 191 | 195 | PF00917 | 0.504 |
DOC_MAPK_gen_1 | 261 | 270 | PF00069 | 0.500 |
DOC_MAPK_gen_1 | 75 | 81 | PF00069 | 0.785 |
DOC_MAPK_MEF2A_6 | 46 | 54 | PF00069 | 0.492 |
DOC_PP2B_LxvP_1 | 255 | 258 | PF13499 | 0.573 |
DOC_PP2B_LxvP_1 | 268 | 271 | PF13499 | 0.405 |
DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.543 |
DOC_USP7_MATH_1 | 191 | 195 | PF00917 | 0.495 |
DOC_USP7_MATH_1 | 207 | 211 | PF00917 | 0.384 |
DOC_WW_Pin1_4 | 101 | 106 | PF00397 | 0.736 |
DOC_WW_Pin1_4 | 11 | 16 | PF00397 | 0.642 |
DOC_WW_Pin1_4 | 372 | 377 | PF00397 | 0.610 |
DOC_WW_Pin1_4 | 389 | 394 | PF00397 | 0.537 |
DOC_WW_Pin1_4 | 70 | 75 | PF00397 | 0.620 |
DOC_WW_Pin1_4 | 80 | 85 | PF00397 | 0.581 |
LIG_14-3-3_CanoR_1 | 199 | 204 | PF00244 | 0.479 |
LIG_14-3-3_CanoR_1 | 261 | 266 | PF00244 | 0.534 |
LIG_14-3-3_CanoR_1 | 372 | 376 | PF00244 | 0.589 |
LIG_14-3-3_CanoR_1 | 75 | 80 | PF00244 | 0.687 |
LIG_Actin_WH2_2 | 248 | 265 | PF00022 | 0.441 |
LIG_AP2alpha_2 | 117 | 119 | PF02296 | 0.560 |
LIG_APCC_ABBA_1 | 116 | 121 | PF00400 | 0.570 |
LIG_CaM_NSCaTE_8 | 305 | 312 | PF13499 | 0.542 |
LIG_CtBP_PxDLS_1 | 137 | 141 | PF00389 | 0.634 |
LIG_CtBP_PxDLS_1 | 220 | 224 | PF00389 | 0.389 |
LIG_eIF4E_1 | 273 | 279 | PF01652 | 0.475 |
LIG_FHA_1 | 207 | 213 | PF00498 | 0.423 |
LIG_FHA_2 | 25 | 31 | PF00498 | 0.421 |
LIG_GBD_Chelix_1 | 238 | 246 | PF00786 | 0.469 |
LIG_LIR_Apic_2 | 149 | 155 | PF02991 | 0.614 |
LIG_LIR_Gen_1 | 240 | 250 | PF02991 | 0.474 |
LIG_LIR_Gen_1 | 27 | 37 | PF02991 | 0.471 |
LIG_LIR_Gen_1 | 329 | 338 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 156 | 160 | PF02991 | 0.573 |
LIG_LIR_Nem_3 | 240 | 246 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 27 | 32 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 329 | 334 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 94 | 100 | PF02991 | 0.674 |
LIG_PCNA_yPIPBox_3 | 249 | 263 | PF02747 | 0.454 |
LIG_SH2_CRK | 331 | 335 | PF00017 | 0.626 |
LIG_SH2_PTP2 | 152 | 155 | PF00017 | 0.569 |
LIG_SH2_PTP2 | 157 | 160 | PF00017 | 0.539 |
LIG_SH2_SRC | 157 | 160 | PF00017 | 0.454 |
LIG_SH2_STAP1 | 243 | 247 | PF00017 | 0.403 |
LIG_SH2_STAP1 | 331 | 335 | PF00017 | 0.510 |
LIG_SH2_STAT3 | 273 | 276 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 125 | 128 | PF00017 | 0.520 |
LIG_SH2_STAT5 | 152 | 155 | PF00017 | 0.569 |
LIG_SH2_STAT5 | 157 | 160 | PF00017 | 0.539 |
LIG_SH2_STAT5 | 243 | 246 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 348 | 351 | PF00017 | 0.464 |
LIG_SH2_STAT5 | 56 | 59 | PF00017 | 0.575 |
LIG_SH3_3 | 200 | 206 | PF00018 | 0.442 |
LIG_SH3_3 | 76 | 82 | PF00018 | 0.634 |
LIG_SUMO_SIM_anti_2 | 264 | 269 | PF11976 | 0.424 |
LIG_SUMO_SIM_par_1 | 136 | 141 | PF11976 | 0.636 |
LIG_SUMO_SIM_par_1 | 348 | 354 | PF11976 | 0.484 |
LIG_TRAF2_1 | 146 | 149 | PF00917 | 0.498 |
LIG_WRC_WIRS_1 | 57 | 62 | PF05994 | 0.423 |
MOD_CDC14_SPxK_1 | 73 | 76 | PF00782 | 0.634 |
MOD_CDK_SPK_2 | 101 | 106 | PF00069 | 0.616 |
MOD_CDK_SPK_2 | 70 | 75 | PF00069 | 0.620 |
MOD_CDK_SPK_2 | 80 | 85 | PF00069 | 0.533 |
MOD_CDK_SPxK_1 | 70 | 76 | PF00069 | 0.623 |
MOD_CDK_SPxxK_3 | 101 | 108 | PF00069 | 0.614 |
MOD_CDK_SPxxK_3 | 70 | 77 | PF00069 | 0.627 |
MOD_CK1_1 | 193 | 199 | PF00069 | 0.561 |
MOD_CK1_1 | 70 | 76 | PF00069 | 0.640 |
MOD_CK2_1 | 11 | 17 | PF00069 | 0.709 |
MOD_CK2_1 | 138 | 144 | PF00069 | 0.562 |
MOD_CK2_1 | 80 | 86 | PF00069 | 0.625 |
MOD_CK2_1 | 88 | 94 | PF00069 | 0.615 |
MOD_Cter_Amidation | 87 | 90 | PF01082 | 0.623 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.473 |
MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.449 |
MOD_GlcNHglycan | 310 | 313 | PF01048 | 0.535 |
MOD_GSK3_1 | 237 | 244 | PF00069 | 0.474 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.591 |
MOD_N-GLC_1 | 207 | 212 | PF02516 | 0.369 |
MOD_NEK2_1 | 176 | 181 | PF00069 | 0.536 |
MOD_NEK2_1 | 19 | 24 | PF00069 | 0.482 |
MOD_NEK2_1 | 190 | 195 | PF00069 | 0.491 |
MOD_NEK2_1 | 279 | 284 | PF00069 | 0.466 |
MOD_NEK2_2 | 56 | 61 | PF00069 | 0.424 |
MOD_PIKK_1 | 313 | 319 | PF00454 | 0.491 |
MOD_PIKK_1 | 329 | 335 | PF00454 | 0.455 |
MOD_PIKK_1 | 4 | 10 | PF00454 | 0.524 |
MOD_PK_1 | 199 | 205 | PF00069 | 0.536 |
MOD_PK_1 | 261 | 267 | PF00069 | 0.458 |
MOD_PK_1 | 75 | 81 | PF00069 | 0.689 |
MOD_PKA_1 | 75 | 81 | PF00069 | 0.779 |
MOD_PKA_2 | 228 | 234 | PF00069 | 0.551 |
MOD_PKA_2 | 371 | 377 | PF00069 | 0.613 |
MOD_PKA_2 | 75 | 81 | PF00069 | 0.713 |
MOD_PKB_1 | 261 | 269 | PF00069 | 0.361 |
MOD_PKB_1 | 293 | 301 | PF00069 | 0.507 |
MOD_PKB_1 | 75 | 83 | PF00069 | 0.820 |
MOD_Plk_1 | 279 | 285 | PF00069 | 0.496 |
MOD_Plk_1 | 298 | 304 | PF00069 | 0.365 |
MOD_Plk_4 | 153 | 159 | PF00069 | 0.627 |
MOD_Plk_4 | 263 | 269 | PF00069 | 0.430 |
MOD_Plk_4 | 279 | 285 | PF00069 | 0.429 |
MOD_ProDKin_1 | 101 | 107 | PF00069 | 0.734 |
MOD_ProDKin_1 | 11 | 17 | PF00069 | 0.641 |
MOD_ProDKin_1 | 372 | 378 | PF00069 | 0.612 |
MOD_ProDKin_1 | 389 | 395 | PF00069 | 0.536 |
MOD_ProDKin_1 | 70 | 76 | PF00069 | 0.623 |
MOD_ProDKin_1 | 80 | 86 | PF00069 | 0.581 |
MOD_SUMO_rev_2 | 139 | 146 | PF00179 | 0.575 |
TRG_ENDOCYTIC_2 | 157 | 160 | PF00928 | 0.575 |
TRG_ENDOCYTIC_2 | 243 | 246 | PF00928 | 0.405 |
TRG_ENDOCYTIC_2 | 331 | 334 | PF00928 | 0.518 |
TRG_ER_diArg_1 | 105 | 108 | PF00400 | 0.736 |
TRG_ER_diArg_1 | 260 | 263 | PF00400 | 0.530 |
TRG_ER_diArg_1 | 41 | 43 | PF00400 | 0.459 |
TRG_ER_diArg_1 | 74 | 77 | PF00400 | 0.684 |
TRG_Pf-PMV_PEXEL_1 | 225 | 230 | PF00026 | 0.477 |
TRG_Pf-PMV_PEXEL_1 | 295 | 299 | PF00026 | 0.537 |
TRG_Pf-PMV_PEXEL_1 | 34 | 38 | PF00026 | 0.537 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IDJ0 | Leishmania donovani | 84% | 100% |
A4H8D4 | Leishmania braziliensis | 65% | 100% |
A4HWQ6 | Leishmania infantum | 84% | 100% |
Q4QF13 | Leishmania major | 82% | 100% |
Q8IS09 | Leptomonas seymouri | 30% | 100% |