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: E9ATR4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 10 | 12 | PF00675 | 0.618 |
CLV_NRD_NRD_1 | 101 | 103 | PF00675 | 0.596 |
CLV_NRD_NRD_1 | 211 | 213 | PF00675 | 0.407 |
CLV_NRD_NRD_1 | 23 | 25 | PF00675 | 0.651 |
CLV_NRD_NRD_1 | 402 | 404 | PF00675 | 0.315 |
CLV_PCSK_FUR_1 | 7 | 11 | PF00082 | 0.572 |
CLV_PCSK_KEX2_1 | 10 | 12 | PF00082 | 0.623 |
CLV_PCSK_KEX2_1 | 21 | 23 | PF00082 | 0.643 |
CLV_PCSK_KEX2_1 | 286 | 288 | PF00082 | 0.508 |
CLV_PCSK_KEX2_1 | 7 | 9 | PF00082 | 0.611 |
CLV_PCSK_KEX2_1 | 78 | 80 | PF00082 | 0.389 |
CLV_PCSK_PC1ET2_1 | 21 | 23 | PF00082 | 0.631 |
CLV_PCSK_PC1ET2_1 | 286 | 288 | PF00082 | 0.508 |
CLV_PCSK_PC1ET2_1 | 78 | 80 | PF00082 | 0.389 |
CLV_PCSK_SKI1_1 | 323 | 327 | PF00082 | 0.414 |
CLV_PCSK_SKI1_1 | 403 | 407 | PF00082 | 0.486 |
CLV_PCSK_SKI1_1 | 52 | 56 | PF00082 | 0.418 |
CLV_PCSK_SKI1_1 | 75 | 79 | PF00082 | 0.416 |
DEG_ODPH_VHL_1 | 4 | 17 | PF01847 | 0.618 |
DEG_SPOP_SBC_1 | 268 | 272 | PF00917 | 0.645 |
DOC_MAPK_DCC_7 | 86 | 96 | PF00069 | 0.368 |
DOC_MAPK_gen_1 | 403 | 413 | PF00069 | 0.250 |
DOC_MAPK_gen_1 | 7 | 17 | PF00069 | 0.592 |
DOC_MAPK_JIP1_4 | 407 | 413 | PF00069 | 0.429 |
DOC_MAPK_MEF2A_6 | 46 | 53 | PF00069 | 0.450 |
DOC_MAPK_NFAT4_5 | 46 | 54 | PF00069 | 0.458 |
DOC_USP7_MATH_1 | 109 | 113 | PF00917 | 0.717 |
DOC_USP7_MATH_1 | 117 | 121 | PF00917 | 0.589 |
DOC_USP7_MATH_1 | 160 | 164 | PF00917 | 0.486 |
DOC_USP7_MATH_1 | 228 | 232 | PF00917 | 0.384 |
DOC_WW_Pin1_4 | 131 | 136 | PF00397 | 0.622 |
DOC_WW_Pin1_4 | 451 | 456 | PF00397 | 0.301 |
LIG_14-3-3_CanoR_1 | 110 | 114 | PF00244 | 0.640 |
LIG_14-3-3_CanoR_1 | 212 | 217 | PF00244 | 0.430 |
LIG_14-3-3_CanoR_1 | 22 | 30 | PF00244 | 0.483 |
LIG_14-3-3_CanoR_1 | 245 | 254 | PF00244 | 0.701 |
LIG_14-3-3_CanoR_1 | 276 | 280 | PF00244 | 0.655 |
LIG_14-3-3_CanoR_1 | 287 | 294 | PF00244 | 0.453 |
LIG_14-3-3_CanoR_1 | 443 | 451 | PF00244 | 0.468 |
LIG_14-3-3_CanoR_1 | 495 | 500 | PF00244 | 0.284 |
LIG_14-3-3_CanoR_1 | 64 | 72 | PF00244 | 0.352 |
LIG_14-3-3_CanoR_1 | 8 | 17 | PF00244 | 0.596 |
LIG_14-3-3_CterR_2 | 507 | 511 | PF00244 | 0.372 |
LIG_Actin_WH2_2 | 190 | 206 | PF00022 | 0.345 |
LIG_Actin_WH2_2 | 76 | 94 | PF00022 | 0.367 |
LIG_FHA_1 | 10 | 16 | PF00498 | 0.571 |
LIG_FHA_1 | 254 | 260 | PF00498 | 0.542 |
LIG_FHA_1 | 263 | 269 | PF00498 | 0.542 |
LIG_FHA_1 | 303 | 309 | PF00498 | 0.446 |
LIG_FHA_1 | 400 | 406 | PF00498 | 0.461 |
LIG_FHA_1 | 53 | 59 | PF00498 | 0.539 |
LIG_FHA_1 | 64 | 70 | PF00498 | 0.291 |
LIG_FHA_2 | 137 | 143 | PF00498 | 0.648 |
LIG_FHA_2 | 163 | 169 | PF00498 | 0.525 |
LIG_FHA_2 | 213 | 219 | PF00498 | 0.347 |
LIG_FHA_2 | 235 | 241 | PF00498 | 0.563 |
LIG_FHA_2 | 348 | 354 | PF00498 | 0.423 |
LIG_FHA_2 | 452 | 458 | PF00498 | 0.404 |
LIG_FHA_2 | 468 | 474 | PF00498 | 0.431 |
LIG_FHA_2 | 96 | 102 | PF00498 | 0.650 |
LIG_GBD_Chelix_1 | 474 | 482 | PF00786 | 0.375 |
LIG_LIR_Apic_2 | 112 | 116 | PF02991 | 0.667 |
LIG_LIR_Gen_1 | 194 | 203 | PF02991 | 0.333 |
LIG_LIR_Gen_1 | 292 | 302 | PF02991 | 0.278 |
LIG_LIR_Gen_1 | 378 | 388 | PF02991 | 0.338 |
LIG_LIR_Nem_3 | 194 | 198 | PF02991 | 0.333 |
LIG_LIR_Nem_3 | 292 | 297 | PF02991 | 0.305 |
LIG_LIR_Nem_3 | 378 | 384 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 473 | 479 | PF02991 | 0.421 |
LIG_MYND_1 | 2 | 6 | PF01753 | 0.623 |
LIG_Pex14_1 | 486 | 490 | PF04695 | 0.331 |
LIG_Pex14_2 | 44 | 48 | PF04695 | 0.431 |
LIG_SH2_CRK | 113 | 117 | PF00017 | 0.566 |
LIG_SH2_CRK | 200 | 204 | PF00017 | 0.414 |
LIG_SH2_CRK | 377 | 381 | PF00017 | 0.326 |
LIG_SH2_CRK | 428 | 432 | PF00017 | 0.441 |
LIG_SH2_NCK_1 | 428 | 432 | PF00017 | 0.441 |
LIG_SH2_STAP1 | 377 | 381 | PF00017 | 0.326 |
LIG_SH2_STAP1 | 428 | 432 | PF00017 | 0.441 |
LIG_SH2_STAP1 | 463 | 467 | PF00017 | 0.376 |
LIG_SH2_STAP1 | 479 | 483 | PF00017 | 0.353 |
LIG_SH2_STAT5 | 148 | 151 | PF00017 | 0.362 |
LIG_SH2_STAT5 | 200 | 203 | PF00017 | 0.409 |
LIG_SH3_1 | 103 | 109 | PF00018 | 0.579 |
LIG_SH3_2 | 3 | 8 | PF14604 | 0.619 |
LIG_SH3_3 | 103 | 109 | PF00018 | 0.539 |
LIG_SUMO_SIM_par_1 | 329 | 336 | PF11976 | 0.356 |
LIG_TRAF2_1 | 215 | 218 | PF00917 | 0.304 |
LIG_TRAF2_1 | 98 | 101 | PF00917 | 0.602 |
LIG_TYR_ITIM | 198 | 203 | PF00017 | 0.409 |
LIG_WRC_WIRS_1 | 192 | 197 | PF05994 | 0.333 |
LIG_WRC_WIRS_1 | 291 | 296 | PF05994 | 0.318 |
LIG_WW_3 | 107 | 111 | PF00397 | 0.669 |
MOD_CK1_1 | 141 | 147 | PF00069 | 0.381 |
MOD_CK1_1 | 167 | 173 | PF00069 | 0.443 |
MOD_CK1_1 | 191 | 197 | PF00069 | 0.468 |
MOD_CK1_1 | 231 | 237 | PF00069 | 0.677 |
MOD_CK1_1 | 289 | 295 | PF00069 | 0.558 |
MOD_CK2_1 | 212 | 218 | PF00069 | 0.431 |
MOD_CK2_1 | 234 | 240 | PF00069 | 0.542 |
MOD_CK2_1 | 247 | 253 | PF00069 | 0.532 |
MOD_CK2_1 | 95 | 101 | PF00069 | 0.642 |
MOD_GlcNHglycan | 119 | 122 | PF01048 | 0.565 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.423 |
MOD_GlcNHglycan | 250 | 253 | PF01048 | 0.767 |
MOD_GlcNHglycan | 260 | 263 | PF01048 | 0.692 |
MOD_GlcNHglycan | 420 | 423 | PF01048 | 0.398 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.516 |
MOD_GSK3_1 | 228 | 235 | PF00069 | 0.633 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.532 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.569 |
MOD_GSK3_1 | 267 | 274 | PF00069 | 0.802 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.474 |
MOD_GSK3_1 | 347 | 354 | PF00069 | 0.499 |
MOD_GSK3_1 | 457 | 464 | PF00069 | 0.398 |
MOD_N-GLC_1 | 131 | 136 | PF02516 | 0.591 |
MOD_N-GLC_1 | 246 | 251 | PF02516 | 0.613 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.641 |
MOD_NEK2_1 | 38 | 43 | PF00069 | 0.367 |
MOD_NEK2_1 | 388 | 393 | PF00069 | 0.365 |
MOD_NEK2_1 | 465 | 470 | PF00069 | 0.355 |
MOD_PIKK_1 | 262 | 268 | PF00454 | 0.635 |
MOD_PIKK_1 | 269 | 275 | PF00454 | 0.684 |
MOD_PIKK_1 | 63 | 69 | PF00454 | 0.411 |
MOD_PKA_1 | 212 | 218 | PF00069 | 0.359 |
MOD_PKA_1 | 23 | 29 | PF00069 | 0.555 |
MOD_PKA_1 | 286 | 292 | PF00069 | 0.467 |
MOD_PKA_1 | 9 | 15 | PF00069 | 0.577 |
MOD_PKA_2 | 109 | 115 | PF00069 | 0.685 |
MOD_PKA_2 | 23 | 29 | PF00069 | 0.522 |
MOD_PKA_2 | 275 | 281 | PF00069 | 0.655 |
MOD_PKA_2 | 286 | 292 | PF00069 | 0.487 |
MOD_PKA_2 | 63 | 69 | PF00069 | 0.364 |
MOD_PKA_2 | 9 | 15 | PF00069 | 0.573 |
MOD_PKB_1 | 7 | 15 | PF00069 | 0.594 |
MOD_Plk_1 | 141 | 147 | PF00069 | 0.386 |
MOD_Plk_1 | 167 | 173 | PF00069 | 0.443 |
MOD_Plk_1 | 289 | 295 | PF00069 | 0.334 |
MOD_Plk_1 | 38 | 44 | PF00069 | 0.371 |
MOD_Plk_2-3 | 461 | 467 | PF00069 | 0.361 |
MOD_Plk_4 | 172 | 178 | PF00069 | 0.384 |
MOD_Plk_4 | 188 | 194 | PF00069 | 0.353 |
MOD_Plk_4 | 275 | 281 | PF00069 | 0.500 |
MOD_Plk_4 | 445 | 451 | PF00069 | 0.369 |
MOD_Plk_4 | 478 | 484 | PF00069 | 0.434 |
MOD_ProDKin_1 | 131 | 137 | PF00069 | 0.621 |
MOD_ProDKin_1 | 451 | 457 | PF00069 | 0.304 |
MOD_SUMO_rev_2 | 13 | 17 | PF00179 | 0.667 |
MOD_SUMO_rev_2 | 278 | 288 | PF00179 | 0.608 |
MOD_SUMO_rev_2 | 353 | 358 | PF00179 | 0.521 |
TRG_ENDOCYTIC_2 | 200 | 203 | PF00928 | 0.409 |
TRG_ENDOCYTIC_2 | 377 | 380 | PF00928 | 0.327 |
TRG_ENDOCYTIC_2 | 381 | 384 | PF00928 | 0.341 |
TRG_ENDOCYTIC_2 | 428 | 431 | PF00928 | 0.371 |
TRG_ENDOCYTIC_2 | 479 | 482 | PF00928 | 0.352 |
TRG_ER_diArg_1 | 22 | 24 | PF00400 | 0.656 |
TRG_ER_diArg_1 | 494 | 497 | PF00400 | 0.377 |
TRG_ER_diArg_1 | 504 | 507 | PF00400 | 0.431 |
TRG_ER_diArg_1 | 6 | 9 | PF00400 | 0.597 |
TRG_NLS_Bipartite_1 | 7 | 25 | PF00514 | 0.563 |
TRG_NLS_MonoCore_2 | 20 | 25 | PF00514 | 0.580 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDJ0 | Leptomonas seymouri | 55% | 100% |
A0A3S7XBN4 | Leishmania donovani | 88% | 100% |
A4HPZ7 | Leishmania braziliensis | 78% | 100% |
A4IDQ8 | Leishmania infantum | 88% | 100% |
Q4Q0T3 | Leishmania major | 87% | 100% |