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: 35 |
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: 4 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: Q9XZX8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_PCSK_KEX2_1 | 121 | 123 | PF00082 | 0.563 |
CLV_PCSK_PC1ET2_1 | 121 | 123 | PF00082 | 0.563 |
CLV_PCSK_SKI1_1 | 154 | 158 | PF00082 | 0.538 |
CLV_PCSK_SKI1_1 | 4 | 8 | PF00082 | 0.716 |
DEG_APCC_DBOX_1 | 121 | 129 | PF00400 | 0.339 |
DEG_APCC_DBOX_1 | 3 | 11 | PF00400 | 0.532 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.557 |
DEG_SCF_FBW7_1 | 317 | 322 | PF00400 | 0.444 |
DOC_ANK_TNKS_1 | 33 | 40 | PF00023 | 0.411 |
DOC_CKS1_1 | 316 | 321 | PF01111 | 0.449 |
DOC_CKS1_1 | 338 | 343 | PF01111 | 0.448 |
DOC_MAPK_gen_1 | 2 | 10 | PF00069 | 0.628 |
DOC_MAPK_MEF2A_6 | 2 | 10 | PF00069 | 0.533 |
DOC_PP1_RVXF_1 | 152 | 158 | PF00149 | 0.340 |
DOC_USP7_MATH_1 | 146 | 150 | PF00917 | 0.439 |
DOC_USP7_MATH_1 | 156 | 160 | PF00917 | 0.328 |
DOC_USP7_MATH_1 | 177 | 181 | PF00917 | 0.366 |
DOC_USP7_MATH_1 | 220 | 224 | PF00917 | 0.374 |
DOC_WW_Pin1_4 | 16 | 21 | PF00397 | 0.658 |
DOC_WW_Pin1_4 | 315 | 320 | PF00397 | 0.453 |
DOC_WW_Pin1_4 | 321 | 326 | PF00397 | 0.397 |
DOC_WW_Pin1_4 | 337 | 342 | PF00397 | 0.320 |
DOC_WW_Pin1_4 | 346 | 351 | PF00397 | 0.362 |
DOC_WW_Pin1_4 | 397 | 402 | PF00397 | 0.444 |
LIG_14-3-3_CanoR_1 | 361 | 369 | PF00244 | 0.406 |
LIG_BRCT_BRCA1_1 | 179 | 183 | PF00533 | 0.376 |
LIG_eIF4E_1 | 315 | 321 | PF01652 | 0.425 |
LIG_FHA_1 | 229 | 235 | PF00498 | 0.346 |
LIG_FHA_1 | 316 | 322 | PF00498 | 0.411 |
LIG_FHA_1 | 376 | 382 | PF00498 | 0.409 |
LIG_FHA_1 | 55 | 61 | PF00498 | 0.460 |
LIG_FHA_1 | 91 | 97 | PF00498 | 0.418 |
LIG_GBD_Chelix_1 | 326 | 334 | PF00786 | 0.637 |
LIG_LIR_Apic_2 | 251 | 257 | PF02991 | 0.369 |
LIG_LIR_Gen_1 | 468 | 479 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 127 | 133 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 354 | 359 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 468 | 474 | PF02991 | 0.429 |
LIG_Pex14_2 | 41 | 45 | PF04695 | 0.340 |
LIG_PTB_Apo_2 | 423 | 430 | PF02174 | 0.432 |
LIG_PTB_Phospho_1 | 423 | 429 | PF10480 | 0.433 |
LIG_SH2_CRK | 254 | 258 | PF00017 | 0.364 |
LIG_SH2_CRK | 356 | 360 | PF00017 | 0.418 |
LIG_SH2_CRK | 471 | 475 | PF00017 | 0.421 |
LIG_SH2_NCK_1 | 471 | 475 | PF00017 | 0.334 |
LIG_SH2_STAP1 | 248 | 252 | PF00017 | 0.392 |
LIG_SH2_STAP1 | 389 | 393 | PF00017 | 0.439 |
LIG_SH2_STAP1 | 486 | 490 | PF00017 | 0.404 |
LIG_SH2_STAT5 | 197 | 200 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.410 |
LIG_SH2_STAT5 | 248 | 251 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 254 | 257 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 316 | 319 | PF00017 | 0.457 |
LIG_SH2_STAT5 | 351 | 354 | PF00017 | 0.406 |
LIG_SH2_STAT5 | 424 | 427 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 430 | 433 | PF00017 | 0.403 |
LIG_SH2_STAT5 | 443 | 446 | PF00017 | 0.318 |
LIG_SH2_STAT5 | 465 | 468 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 95 | 98 | PF00017 | 0.447 |
LIG_SH3_2 | 338 | 343 | PF14604 | 0.448 |
LIG_SH3_3 | 335 | 341 | PF00018 | 0.442 |
LIG_SH3_3 | 47 | 53 | PF00018 | 0.451 |
LIG_SH3_3 | 70 | 76 | PF00018 | 0.404 |
LIG_SH3_3 | 93 | 99 | PF00018 | 0.391 |
LIG_TRFH_1 | 315 | 319 | PF08558 | 0.446 |
LIG_TRFH_1 | 95 | 99 | PF08558 | 0.390 |
LIG_TYR_ITIM | 128 | 133 | PF00017 | 0.348 |
LIG_WRC_WIRS_1 | 496 | 501 | PF05994 | 0.298 |
MOD_CDK_SPxK_1 | 337 | 343 | PF00069 | 0.444 |
MOD_CK1_1 | 144 | 150 | PF00069 | 0.434 |
MOD_CK1_1 | 268 | 274 | PF00069 | 0.459 |
MOD_CK1_1 | 300 | 306 | PF00069 | 0.417 |
MOD_CK1_1 | 397 | 403 | PF00069 | 0.445 |
MOD_CK1_1 | 469 | 475 | PF00069 | 0.344 |
MOD_CK1_1 | 74 | 80 | PF00069 | 0.375 |
MOD_CK2_1 | 113 | 119 | PF00069 | 0.395 |
MOD_CK2_1 | 131 | 137 | PF00069 | 0.322 |
MOD_Cter_Amidation | 119 | 122 | PF01082 | 0.593 |
MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.583 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.544 |
MOD_GlcNHglycan | 213 | 216 | PF01048 | 0.535 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.502 |
MOD_GlcNHglycan | 222 | 225 | PF01048 | 0.521 |
MOD_GlcNHglycan | 391 | 394 | PF01048 | 0.578 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.594 |
MOD_GlcNHglycan | 480 | 483 | PF01048 | 0.640 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.634 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.355 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.354 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.336 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.333 |
MOD_GSK3_1 | 236 | 243 | PF00069 | 0.292 |
MOD_GSK3_1 | 268 | 275 | PF00069 | 0.465 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.445 |
MOD_GSK3_1 | 360 | 367 | PF00069 | 0.393 |
MOD_GSK3_1 | 389 | 396 | PF00069 | 0.422 |
MOD_GSK3_1 | 452 | 459 | PF00069 | 0.441 |
MOD_GSK3_1 | 465 | 472 | PF00069 | 0.363 |
MOD_N-GLC_1 | 199 | 204 | PF02516 | 0.526 |
MOD_N-GLC_2 | 101 | 103 | PF02516 | 0.560 |
MOD_N-GLC_2 | 104 | 106 | PF02516 | 0.565 |
MOD_N-GLC_2 | 27 | 29 | PF02516 | 0.549 |
MOD_N-GLC_2 | 306 | 308 | PF02516 | 0.589 |
MOD_N-GLC_2 | 412 | 414 | PF02516 | 0.636 |
MOD_NEK2_1 | 157 | 162 | PF00069 | 0.388 |
MOD_NEK2_1 | 195 | 200 | PF00069 | 0.370 |
MOD_NEK2_1 | 452 | 457 | PF00069 | 0.454 |
MOD_NEK2_1 | 466 | 471 | PF00069 | 0.343 |
MOD_NEK2_1 | 495 | 500 | PF00069 | 0.404 |
MOD_OFUCOSY | 269 | 276 | PF10250 | 0.653 |
MOD_OFUCOSY | 72 | 78 | PF10250 | 0.580 |
MOD_PIKK_1 | 141 | 147 | PF00454 | 0.433 |
MOD_PIKK_1 | 274 | 280 | PF00454 | 0.423 |
MOD_PIKK_1 | 306 | 312 | PF00454 | 0.393 |
MOD_PIKK_1 | 400 | 406 | PF00454 | 0.459 |
MOD_PIKK_1 | 472 | 478 | PF00454 | 0.423 |
MOD_PKA_2 | 360 | 366 | PF00069 | 0.404 |
MOD_Plk_4 | 37 | 43 | PF00069 | 0.408 |
MOD_Plk_4 | 484 | 490 | PF00069 | 0.420 |
MOD_ProDKin_1 | 16 | 22 | PF00069 | 0.653 |
MOD_ProDKin_1 | 315 | 321 | PF00069 | 0.451 |
MOD_ProDKin_1 | 337 | 343 | PF00069 | 0.444 |
MOD_ProDKin_1 | 346 | 352 | PF00069 | 0.362 |
MOD_ProDKin_1 | 397 | 403 | PF00069 | 0.452 |
TRG_DiLeu_BaLyEn_6 | 316 | 321 | PF01217 | 0.414 |
TRG_ENDOCYTIC_2 | 130 | 133 | PF00928 | 0.418 |
TRG_ENDOCYTIC_2 | 283 | 286 | PF00928 | 0.408 |
TRG_ENDOCYTIC_2 | 356 | 359 | PF00928 | 0.424 |
TRG_ENDOCYTIC_2 | 471 | 474 | PF00928 | 0.420 |
TRG_ER_diArg_1 | 1 | 4 | PF00400 | 0.652 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S5H584 | Leishmania donovani | 93% | 100% |
A0A451EJW6 | Leishmania donovani | 71% | 71% |
A4H3U2 | Leishmania braziliensis | 65% | 100% |
A4H3Y2 | Leishmania braziliensis | 31% | 88% |
A4HS13 | Leishmania infantum | 94% | 100% |
A4HS14 | Leishmania infantum | 71% | 71% |
E9AK00 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
E9AK01 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 67% | 71% |
Q9XZX9 | Leishmania major | 73% | 71% |