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. | yes | yes: 20 |
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 | yes | yes: 6, no: 0 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: E9AYP9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 339 | 343 | PF00656 | 0.464 |
CLV_NRD_NRD_1 | 202 | 204 | PF00675 | 0.519 |
CLV_PCSK_SKI1_1 | 204 | 208 | PF00082 | 0.566 |
DEG_ODPH_VHL_1 | 44 | 56 | PF01847 | 0.547 |
DEG_SPOP_SBC_1 | 56 | 60 | PF00917 | 0.540 |
DOC_CKS1_1 | 155 | 160 | PF01111 | 0.417 |
DOC_MAPK_gen_1 | 203 | 211 | PF00069 | 0.481 |
DOC_MAPK_MEF2A_6 | 203 | 211 | PF00069 | 0.481 |
DOC_PP1_RVXF_1 | 206 | 212 | PF00149 | 0.430 |
DOC_PP4_FxxP_1 | 67 | 70 | PF00568 | 0.402 |
DOC_USP7_MATH_1 | 210 | 214 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 252 | 256 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 296 | 300 | PF00917 | 0.519 |
DOC_WW_Pin1_4 | 154 | 159 | PF00397 | 0.444 |
DOC_WW_Pin1_4 | 34 | 39 | PF00397 | 0.589 |
LIG_14-3-3_CanoR_1 | 112 | 117 | PF00244 | 0.519 |
LIG_14-3-3_CanoR_1 | 33 | 41 | PF00244 | 0.460 |
LIG_14-3-3_CanoR_1 | 72 | 81 | PF00244 | 0.486 |
LIG_APCC_ABBAyCdc20_2 | 277 | 283 | PF00400 | 0.510 |
LIG_BRCT_BRCA1_1 | 217 | 221 | PF00533 | 0.507 |
LIG_FHA_1 | 150 | 156 | PF00498 | 0.492 |
LIG_FHA_1 | 157 | 163 | PF00498 | 0.473 |
LIG_FHA_1 | 18 | 24 | PF00498 | 0.533 |
LIG_FHA_1 | 215 | 221 | PF00498 | 0.641 |
LIG_FHA_1 | 255 | 261 | PF00498 | 0.660 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.663 |
LIG_FHA_1 | 58 | 64 | PF00498 | 0.593 |
LIG_FHA_1 | 74 | 80 | PF00498 | 0.496 |
LIG_FHA_2 | 337 | 343 | PF00498 | 0.463 |
LIG_FHA_2 | 365 | 371 | PF00498 | 0.425 |
LIG_FHA_2 | 57 | 63 | PF00498 | 0.532 |
LIG_GBD_Chelix_1 | 8 | 16 | PF00786 | 0.517 |
LIG_LIR_Gen_1 | 299 | 307 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 159 | 164 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 299 | 303 | PF02991 | 0.552 |
LIG_LIR_Nem_3 | 358 | 364 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 370 | 376 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 95 | 100 | PF02991 | 0.508 |
LIG_LYPXL_yS_3 | 164 | 167 | PF13949 | 0.515 |
LIG_PTB_Apo_2 | 325 | 332 | PF02174 | 0.430 |
LIG_SH2_CRK | 124 | 128 | PF00017 | 0.494 |
LIG_SH2_CRK | 183 | 187 | PF00017 | 0.524 |
LIG_SH2_CRK | 300 | 304 | PF00017 | 0.577 |
LIG_SH2_SRC | 26 | 29 | PF00017 | 0.581 |
LIG_SH2_SRC | 373 | 376 | PF00017 | 0.448 |
LIG_SH2_STAP1 | 225 | 229 | PF00017 | 0.586 |
LIG_SH2_STAP1 | 233 | 237 | PF00017 | 0.459 |
LIG_SH2_STAP1 | 300 | 304 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 179 | 182 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 373 | 376 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 7 | 10 | PF00017 | 0.712 |
LIG_SH3_3 | 264 | 270 | PF00018 | 0.521 |
LIG_SUMO_SIM_anti_2 | 228 | 233 | PF11976 | 0.569 |
LIG_SUMO_SIM_anti_2 | 62 | 67 | PF11976 | 0.486 |
LIG_TYR_ITIM | 162 | 167 | PF00017 | 0.524 |
LIG_TYR_ITIM | 298 | 303 | PF00017 | 0.461 |
LIG_Vh1_VBS_1 | 116 | 134 | PF01044 | 0.393 |
MOD_CK1_1 | 190 | 196 | PF00069 | 0.556 |
MOD_CK1_1 | 255 | 261 | PF00069 | 0.595 |
MOD_CK1_1 | 57 | 63 | PF00069 | 0.520 |
MOD_CK2_1 | 56 | 62 | PF00069 | 0.594 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.503 |
MOD_GlcNHglycan | 222 | 225 | PF01048 | 0.609 |
MOD_GlcNHglycan | 248 | 251 | PF01048 | 0.524 |
MOD_GlcNHglycan | 345 | 348 | PF01048 | 0.573 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.505 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.571 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.388 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.559 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.432 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.468 |
MOD_GSK3_1 | 341 | 348 | PF00069 | 0.547 |
MOD_GSK3_1 | 351 | 358 | PF00069 | 0.418 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.552 |
MOD_N-GLC_1 | 100 | 105 | PF02516 | 0.462 |
MOD_N-GLC_1 | 246 | 251 | PF02516 | 0.579 |
MOD_N-GLC_1 | 253 | 258 | PF02516 | 0.565 |
MOD_N-GLC_1 | 354 | 359 | PF02516 | 0.616 |
MOD_N-GLC_1 | 92 | 97 | PF02516 | 0.472 |
MOD_N-GLC_2 | 143 | 145 | PF02516 | 0.518 |
MOD_NEK2_1 | 100 | 105 | PF00069 | 0.542 |
MOD_NEK2_1 | 11 | 16 | PF00069 | 0.507 |
MOD_NEK2_1 | 125 | 130 | PF00069 | 0.558 |
MOD_NEK2_1 | 220 | 225 | PF00069 | 0.535 |
MOD_NEK2_1 | 246 | 251 | PF00069 | 0.475 |
MOD_NEK2_1 | 311 | 316 | PF00069 | 0.510 |
MOD_NEK2_1 | 341 | 346 | PF00069 | 0.472 |
MOD_NEK2_1 | 363 | 368 | PF00069 | 0.493 |
MOD_NEK2_1 | 54 | 59 | PF00069 | 0.543 |
MOD_NEK2_2 | 284 | 289 | PF00069 | 0.566 |
MOD_PIKK_1 | 110 | 116 | PF00454 | 0.537 |
MOD_PKA_2 | 125 | 131 | PF00069 | 0.498 |
MOD_PKA_2 | 215 | 221 | PF00069 | 0.635 |
MOD_PKA_2 | 32 | 38 | PF00069 | 0.560 |
MOD_Plk_1 | 341 | 347 | PF00069 | 0.474 |
MOD_Plk_1 | 354 | 360 | PF00069 | 0.512 |
MOD_Plk_1 | 92 | 98 | PF00069 | 0.522 |
MOD_Plk_2-3 | 336 | 342 | PF00069 | 0.461 |
MOD_Plk_4 | 112 | 118 | PF00069 | 0.713 |
MOD_Plk_4 | 175 | 181 | PF00069 | 0.438 |
MOD_Plk_4 | 210 | 216 | PF00069 | 0.685 |
MOD_Plk_4 | 336 | 342 | PF00069 | 0.500 |
MOD_Plk_4 | 92 | 98 | PF00069 | 0.657 |
MOD_ProDKin_1 | 154 | 160 | PF00069 | 0.447 |
MOD_ProDKin_1 | 34 | 40 | PF00069 | 0.588 |
TRG_ENDOCYTIC_2 | 124 | 127 | PF00928 | 0.685 |
TRG_ENDOCYTIC_2 | 164 | 167 | PF00928 | 0.515 |
TRG_ENDOCYTIC_2 | 183 | 186 | PF00928 | 0.530 |
TRG_ENDOCYTIC_2 | 300 | 303 | PF00928 | 0.578 |
TRG_ENDOCYTIC_2 | 373 | 376 | PF00928 | 0.448 |
TRG_ENDOCYTIC_2 | 97 | 100 | PF00928 | 0.638 |
TRG_NES_CRM1_1 | 69 | 83 | PF08389 | 0.457 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCM7 | Leptomonas seymouri | 42% | 100% |
A0A3Q8IHC1 | Leishmania donovani | 91% | 100% |
A4HFB2 | Leishmania braziliensis | 72% | 100% |
A4I2J4 | Leishmania infantum | 91% | 100% |
Q4Q8S3 | Leishmania major | 88% | 100% |