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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: Q4QBN1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 102 | 104 | PF00675 | 0.652 |
CLV_NRD_NRD_1 | 19 | 21 | PF00675 | 0.557 |
CLV_PCSK_KEX2_1 | 102 | 104 | PF00082 | 0.652 |
CLV_PCSK_KEX2_1 | 19 | 21 | PF00082 | 0.557 |
CLV_PCSK_KEX2_1 | 65 | 67 | PF00082 | 0.507 |
CLV_PCSK_PC1ET2_1 | 65 | 67 | PF00082 | 0.566 |
CLV_PCSK_SKI1_1 | 305 | 309 | PF00082 | 0.449 |
CLV_PCSK_SKI1_1 | 327 | 331 | PF00082 | 0.515 |
CLV_PCSK_SKI1_1 | 417 | 421 | PF00082 | 0.543 |
CLV_PCSK_SKI1_1 | 87 | 91 | PF00082 | 0.702 |
DEG_APCC_DBOX_1 | 21 | 29 | PF00400 | 0.567 |
DOC_CKS1_1 | 88 | 93 | PF01111 | 0.690 |
DOC_CYCLIN_RxL_1 | 299 | 312 | PF00134 | 0.425 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 54 | 63 | PF00134 | 0.445 |
DOC_CYCLIN_yCln2_LP_2 | 189 | 195 | PF00134 | 0.549 |
DOC_MAPK_gen_1 | 268 | 276 | PF00069 | 0.515 |
DOC_PP1_RVXF_1 | 205 | 211 | PF00149 | 0.505 |
DOC_USP7_MATH_1 | 117 | 121 | PF00917 | 0.707 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.729 |
DOC_USP7_MATH_1 | 181 | 185 | PF00917 | 0.582 |
DOC_USP7_MATH_1 | 259 | 263 | PF00917 | 0.662 |
DOC_WW_Pin1_4 | 130 | 135 | PF00397 | 0.732 |
DOC_WW_Pin1_4 | 141 | 146 | PF00397 | 0.602 |
DOC_WW_Pin1_4 | 282 | 287 | PF00397 | 0.494 |
DOC_WW_Pin1_4 | 348 | 353 | PF00397 | 0.524 |
DOC_WW_Pin1_4 | 373 | 378 | PF00397 | 0.520 |
DOC_WW_Pin1_4 | 87 | 92 | PF00397 | 0.621 |
LIG_14-3-3_CanoR_1 | 113 | 117 | PF00244 | 0.691 |
LIG_14-3-3_CanoR_1 | 140 | 145 | PF00244 | 0.666 |
LIG_14-3-3_CanoR_1 | 212 | 216 | PF00244 | 0.597 |
LIG_14-3-3_CanoR_1 | 282 | 286 | PF00244 | 0.436 |
LIG_14-3-3_CanoR_1 | 345 | 349 | PF00244 | 0.519 |
LIG_14-3-3_CanoR_1 | 439 | 444 | PF00244 | 0.538 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.702 |
LIG_FHA_1 | 16 | 22 | PF00498 | 0.544 |
LIG_FHA_1 | 170 | 176 | PF00498 | 0.406 |
LIG_FHA_1 | 211 | 217 | PF00498 | 0.579 |
LIG_FHA_1 | 309 | 315 | PF00498 | 0.438 |
LIG_FHA_1 | 37 | 43 | PF00498 | 0.564 |
LIG_FHA_1 | 382 | 388 | PF00498 | 0.445 |
LIG_FHA_1 | 418 | 424 | PF00498 | 0.534 |
LIG_FHA_1 | 49 | 55 | PF00498 | 0.455 |
LIG_FHA_1 | 9 | 15 | PF00498 | 0.592 |
LIG_FHA_2 | 304 | 310 | PF00498 | 0.435 |
LIG_FHA_2 | 31 | 37 | PF00498 | 0.665 |
LIG_FHA_2 | 411 | 417 | PF00498 | 0.561 |
LIG_FHA_2 | 440 | 446 | PF00498 | 0.569 |
LIG_FHA_2 | 88 | 94 | PF00498 | 0.696 |
LIG_GBD_Chelix_1 | 216 | 224 | PF00786 | 0.555 |
LIG_LIR_Apic_2 | 239 | 243 | PF02991 | 0.519 |
LIG_LIR_Apic_2 | 347 | 352 | PF02991 | 0.531 |
LIG_LIR_Apic_2 | 51 | 55 | PF02991 | 0.375 |
LIG_LIR_Gen_1 | 442 | 451 | PF02991 | 0.587 |
LIG_LIR_Nem_3 | 223 | 229 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 362 | 368 | PF02991 | 0.427 |
LIG_LIR_Nem_3 | 442 | 446 | PF02991 | 0.573 |
LIG_LIR_Nem_3 | 51 | 56 | PF02991 | 0.400 |
LIG_PALB2_WD40_1 | 48 | 56 | PF16756 | 0.452 |
LIG_Pex14_2 | 365 | 369 | PF04695 | 0.389 |
LIG_PTB_Apo_2 | 239 | 246 | PF02174 | 0.498 |
LIG_PTB_Apo_2 | 55 | 62 | PF02174 | 0.441 |
LIG_PTB_Phospho_1 | 239 | 245 | PF10480 | 0.505 |
LIG_PTB_Phospho_1 | 55 | 61 | PF10480 | 0.441 |
LIG_SH2_CRK | 240 | 244 | PF00017 | 0.509 |
LIG_SH2_CRK | 283 | 287 | PF00017 | 0.373 |
LIG_SH2_GRB2like | 157 | 160 | PF00017 | 0.630 |
LIG_SH2_NCK_1 | 283 | 287 | PF00017 | 0.373 |
LIG_SH2_STAP1 | 443 | 447 | PF00017 | 0.601 |
LIG_SH2_STAT5 | 157 | 160 | PF00017 | 0.595 |
LIG_SH2_STAT5 | 245 | 248 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 27 | 30 | PF00017 | 0.667 |
LIG_SH2_STAT5 | 283 | 286 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 372 | 375 | PF00017 | 0.445 |
LIG_SH2_STAT5 | 61 | 64 | PF00017 | 0.526 |
LIG_SH3_3 | 26 | 32 | PF00018 | 0.589 |
LIG_SH3_3 | 349 | 355 | PF00018 | 0.526 |
LIG_SH3_3 | 375 | 381 | PF00018 | 0.429 |
LIG_SH3_3 | 78 | 84 | PF00018 | 0.677 |
LIG_SH3_3 | 85 | 91 | PF00018 | 0.750 |
LIG_UBA3_1 | 233 | 241 | PF00899 | 0.514 |
MOD_CDC14_SPxK_1 | 137 | 140 | PF00782 | 0.612 |
MOD_CDK_SPxK_1 | 134 | 140 | PF00069 | 0.608 |
MOD_CK1_1 | 133 | 139 | PF00069 | 0.691 |
MOD_CK1_1 | 143 | 149 | PF00069 | 0.618 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.689 |
MOD_CK1_1 | 219 | 225 | PF00069 | 0.591 |
MOD_CK1_1 | 350 | 356 | PF00069 | 0.494 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.544 |
MOD_CK1_1 | 410 | 416 | PF00069 | 0.558 |
MOD_CK2_1 | 143 | 149 | PF00069 | 0.666 |
MOD_CK2_1 | 181 | 187 | PF00069 | 0.464 |
MOD_CK2_1 | 364 | 370 | PF00069 | 0.517 |
MOD_CK2_1 | 415 | 421 | PF00069 | 0.540 |
MOD_CK2_1 | 439 | 445 | PF00069 | 0.618 |
MOD_CK2_1 | 87 | 93 | PF00069 | 0.673 |
MOD_GlcNHglycan | 119 | 122 | PF01048 | 0.710 |
MOD_GlcNHglycan | 246 | 249 | PF01048 | 0.498 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.702 |
MOD_GlcNHglycan | 322 | 325 | PF01048 | 0.409 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.745 |
MOD_GlcNHglycan | 409 | 412 | PF01048 | 0.564 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.641 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.598 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.531 |
MOD_GSK3_1 | 303 | 310 | PF00069 | 0.491 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.529 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.485 |
MOD_N-GLC_1 | 320 | 325 | PF02516 | 0.407 |
MOD_NEK2_1 | 112 | 117 | PF00069 | 0.704 |
MOD_NEK2_1 | 216 | 221 | PF00069 | 0.510 |
MOD_NEK2_1 | 307 | 312 | PF00069 | 0.497 |
MOD_NEK2_1 | 339 | 344 | PF00069 | 0.489 |
MOD_NEK2_2 | 196 | 201 | PF00069 | 0.431 |
MOD_PK_1 | 103 | 109 | PF00069 | 0.654 |
MOD_PK_1 | 232 | 238 | PF00069 | 0.483 |
MOD_PKA_2 | 112 | 118 | PF00069 | 0.701 |
MOD_PKA_2 | 139 | 145 | PF00069 | 0.667 |
MOD_PKA_2 | 15 | 21 | PF00069 | 0.596 |
MOD_PKA_2 | 211 | 217 | PF00069 | 0.588 |
MOD_PKA_2 | 281 | 287 | PF00069 | 0.424 |
MOD_PKA_2 | 344 | 350 | PF00069 | 0.520 |
MOD_Plk_1 | 320 | 326 | PF00069 | 0.413 |
MOD_Plk_1 | 390 | 396 | PF00069 | 0.465 |
MOD_Plk_1 | 415 | 421 | PF00069 | 0.534 |
MOD_Plk_1 | 92 | 98 | PF00069 | 0.642 |
MOD_Plk_2-3 | 364 | 370 | PF00069 | 0.450 |
MOD_Plk_4 | 103 | 109 | PF00069 | 0.690 |
MOD_Plk_4 | 161 | 167 | PF00069 | 0.527 |
MOD_Plk_4 | 169 | 175 | PF00069 | 0.393 |
MOD_Plk_4 | 181 | 187 | PF00069 | 0.399 |
MOD_Plk_4 | 211 | 217 | PF00069 | 0.560 |
MOD_Plk_4 | 303 | 309 | PF00069 | 0.421 |
MOD_Plk_4 | 339 | 345 | PF00069 | 0.487 |
MOD_Plk_4 | 364 | 370 | PF00069 | 0.393 |
MOD_Plk_4 | 381 | 387 | PF00069 | 0.263 |
MOD_Plk_4 | 390 | 396 | PF00069 | 0.404 |
MOD_Plk_4 | 48 | 54 | PF00069 | 0.369 |
MOD_ProDKin_1 | 130 | 136 | PF00069 | 0.732 |
MOD_ProDKin_1 | 141 | 147 | PF00069 | 0.601 |
MOD_ProDKin_1 | 282 | 288 | PF00069 | 0.491 |
MOD_ProDKin_1 | 348 | 354 | PF00069 | 0.519 |
MOD_ProDKin_1 | 373 | 379 | PF00069 | 0.525 |
MOD_ProDKin_1 | 87 | 93 | PF00069 | 0.620 |
MOD_SUMO_for_1 | 298 | 301 | PF00179 | 0.461 |
MOD_SUMO_rev_2 | 235 | 243 | PF00179 | 0.516 |
TRG_DiLeu_BaLyEn_6 | 185 | 190 | PF01217 | 0.518 |
TRG_ENDOCYTIC_2 | 27 | 30 | PF00928 | 0.695 |
TRG_ENDOCYTIC_2 | 431 | 434 | PF00928 | 0.502 |
TRG_ENDOCYTIC_2 | 443 | 446 | PF00928 | 0.517 |
TRG_ER_diArg_1 | 19 | 22 | PF00400 | 0.559 |
TRG_Pf-PMV_PEXEL_1 | 19 | 23 | PF00026 | 0.665 |
TRG_Pf-PMV_PEXEL_1 | 417 | 421 | PF00026 | 0.519 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P811 | Leptomonas seymouri | 80% | 100% |
A0A0S4JBD1 | Bodo saltans | 47% | 100% |
A0A3R7MFR3 | Trypanosoma rangeli | 54% | 100% |
A0A3S7WX76 | Leishmania donovani | 94% | 100% |
A4HCF8 | Leishmania braziliensis | 90% | 100% |
A4HZY7 | Leishmania infantum | 94% | 94% |
E9AVU8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
V5BVW6 | Trypanosoma cruzi | 52% | 100% |