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: A4HUU5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 13 | 15 | PF00675 | 0.675 |
CLV_NRD_NRD_1 | 17 | 19 | PF00675 | 0.666 |
CLV_NRD_NRD_1 | 4 | 6 | PF00675 | 0.675 |
CLV_NRD_NRD_1 | 427 | 429 | PF00675 | 0.578 |
CLV_PCSK_KEX2_1 | 13 | 15 | PF00082 | 0.636 |
CLV_PCSK_KEX2_1 | 360 | 362 | PF00082 | 0.621 |
CLV_PCSK_KEX2_1 | 4 | 6 | PF00082 | 0.661 |
CLV_PCSK_KEX2_1 | 426 | 428 | PF00082 | 0.633 |
CLV_PCSK_PC1ET2_1 | 360 | 362 | PF00082 | 0.561 |
CLV_PCSK_PC1ET2_1 | 4 | 6 | PF00082 | 0.637 |
CLV_PCSK_PC1ET2_1 | 426 | 428 | PF00082 | 0.633 |
DEG_SIAH_1 | 441 | 449 | PF03145 | 0.615 |
DEG_SPOP_SBC_1 | 232 | 236 | PF00917 | 0.644 |
DOC_CKS1_1 | 128 | 133 | PF01111 | 0.670 |
DOC_USP7_MATH_1 | 109 | 113 | PF00917 | 0.749 |
DOC_USP7_MATH_1 | 278 | 282 | PF00917 | 0.648 |
DOC_USP7_MATH_1 | 291 | 295 | PF00917 | 0.655 |
DOC_USP7_MATH_1 | 386 | 390 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 405 | 409 | PF00917 | 0.606 |
DOC_USP7_UBL2_3 | 100 | 104 | PF12436 | 0.605 |
DOC_USP7_UBL2_3 | 6 | 10 | PF12436 | 0.672 |
DOC_WW_Pin1_4 | 127 | 132 | PF00397 | 0.682 |
DOC_WW_Pin1_4 | 162 | 167 | PF00397 | 0.718 |
DOC_WW_Pin1_4 | 214 | 219 | PF00397 | 0.563 |
DOC_WW_Pin1_4 | 220 | 225 | PF00397 | 0.542 |
DOC_WW_Pin1_4 | 233 | 238 | PF00397 | 0.597 |
DOC_WW_Pin1_4 | 273 | 278 | PF00397 | 0.640 |
DOC_WW_Pin1_4 | 351 | 356 | PF00397 | 0.763 |
DOC_WW_Pin1_4 | 362 | 367 | PF00397 | 0.777 |
DOC_WW_Pin1_4 | 369 | 374 | PF00397 | 0.621 |
DOC_WW_Pin1_4 | 79 | 84 | PF00397 | 0.622 |
LIG_14-3-3_CanoR_1 | 136 | 140 | PF00244 | 0.732 |
LIG_14-3-3_CanoR_1 | 61 | 70 | PF00244 | 0.598 |
LIG_14-3-3_CterR_2 | 466 | 470 | PF00244 | 0.564 |
LIG_Actin_WH2_2 | 190 | 206 | PF00022 | 0.566 |
LIG_Actin_WH2_2 | 305 | 322 | PF00022 | 0.545 |
LIG_BIR_III_4 | 250 | 254 | PF00653 | 0.488 |
LIG_Clathr_ClatBox_1 | 263 | 267 | PF01394 | 0.640 |
LIG_FHA_1 | 118 | 124 | PF00498 | 0.657 |
LIG_FHA_1 | 240 | 246 | PF00498 | 0.613 |
LIG_FHA_1 | 346 | 352 | PF00498 | 0.555 |
LIG_FHA_2 | 128 | 134 | PF00498 | 0.662 |
LIG_FHA_2 | 291 | 297 | PF00498 | 0.508 |
LIG_GBD_Chelix_1 | 179 | 187 | PF00786 | 0.549 |
LIG_HP1_1 | 448 | 452 | PF01393 | 0.654 |
LIG_LIR_Apic_2 | 296 | 302 | PF02991 | 0.563 |
LIG_LIR_Apic_2 | 411 | 416 | PF02991 | 0.562 |
LIG_LIR_Gen_1 | 307 | 315 | PF02991 | 0.443 |
LIG_LIR_Gen_1 | 348 | 357 | PF02991 | 0.625 |
LIG_LIR_Nem_3 | 175 | 181 | PF02991 | 0.584 |
LIG_LIR_Nem_3 | 196 | 201 | PF02991 | 0.657 |
LIG_LIR_Nem_3 | 296 | 301 | PF02991 | 0.561 |
LIG_LIR_Nem_3 | 307 | 313 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 348 | 353 | PF02991 | 0.679 |
LIG_SH2_CRK | 125 | 129 | PF00017 | 0.641 |
LIG_SH2_CRK | 413 | 417 | PF00017 | 0.576 |
LIG_SH2_NCK_1 | 125 | 129 | PF00017 | 0.641 |
LIG_SH2_STAT5 | 178 | 181 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 417 | 420 | PF00017 | 0.523 |
LIG_SH2_STAT5 | 47 | 50 | PF00017 | 0.691 |
LIG_SH3_1 | 125 | 131 | PF00018 | 0.637 |
LIG_SH3_3 | 125 | 131 | PF00018 | 0.734 |
LIG_SH3_3 | 153 | 159 | PF00018 | 0.691 |
LIG_SH3_3 | 321 | 327 | PF00018 | 0.599 |
LIG_SUMO_SIM_par_1 | 261 | 267 | PF11976 | 0.584 |
LIG_TRFH_1 | 256 | 260 | PF08558 | 0.499 |
LIG_TRFH_1 | 298 | 302 | PF08558 | 0.473 |
LIG_WW_3 | 322 | 326 | PF00397 | 0.600 |
MOD_CDK_SPK_2 | 364 | 369 | PF00069 | 0.727 |
MOD_CDK_SPxxK_3 | 351 | 358 | PF00069 | 0.625 |
MOD_CDK_SPxxK_3 | 362 | 369 | PF00069 | 0.675 |
MOD_CK1_1 | 118 | 124 | PF00069 | 0.753 |
MOD_CK1_1 | 138 | 144 | PF00069 | 0.620 |
MOD_CK1_1 | 188 | 194 | PF00069 | 0.699 |
MOD_CK1_1 | 202 | 208 | PF00069 | 0.535 |
MOD_CK1_1 | 233 | 239 | PF00069 | 0.635 |
MOD_CK1_1 | 262 | 268 | PF00069 | 0.599 |
MOD_CK1_1 | 279 | 285 | PF00069 | 0.647 |
MOD_CK1_1 | 389 | 395 | PF00069 | 0.590 |
MOD_CK1_1 | 408 | 414 | PF00069 | 0.622 |
MOD_CK1_1 | 54 | 60 | PF00069 | 0.769 |
MOD_CK2_1 | 79 | 85 | PF00069 | 0.653 |
MOD_DYRK1A_RPxSP_1 | 369 | 373 | PF00069 | 0.584 |
MOD_GlcNHglycan | 111 | 114 | PF01048 | 0.760 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.677 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.524 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.522 |
MOD_GlcNHglycan | 293 | 296 | PF01048 | 0.615 |
MOD_GlcNHglycan | 428 | 431 | PF01048 | 0.702 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.763 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.684 |
MOD_GSK3_1 | 181 | 188 | PF00069 | 0.555 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.547 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.559 |
MOD_GSK3_1 | 279 | 286 | PF00069 | 0.626 |
MOD_GSK3_1 | 389 | 396 | PF00069 | 0.730 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.673 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.512 |
MOD_N-GLC_1 | 188 | 193 | PF02516 | 0.593 |
MOD_N-GLC_1 | 70 | 75 | PF02516 | 0.610 |
MOD_NEK2_1 | 123 | 128 | PF00069 | 0.650 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.614 |
MOD_NEK2_1 | 305 | 310 | PF00069 | 0.511 |
MOD_NEK2_1 | 52 | 57 | PF00069 | 0.703 |
MOD_NEK2_2 | 199 | 204 | PF00069 | 0.557 |
MOD_OFUCOSY | 157 | 164 | PF10250 | 0.598 |
MOD_PIKK_1 | 386 | 392 | PF00454 | 0.629 |
MOD_PIKK_1 | 408 | 414 | PF00454 | 0.539 |
MOD_PIKK_1 | 94 | 100 | PF00454 | 0.598 |
MOD_PKA_1 | 426 | 432 | PF00069 | 0.635 |
MOD_PKA_2 | 135 | 141 | PF00069 | 0.699 |
MOD_PKA_2 | 426 | 432 | PF00069 | 0.635 |
MOD_Plk_1 | 188 | 194 | PF00069 | 0.564 |
MOD_Plk_4 | 145 | 151 | PF00069 | 0.716 |
MOD_Plk_4 | 193 | 199 | PF00069 | 0.545 |
MOD_Plk_4 | 259 | 265 | PF00069 | 0.542 |
MOD_Plk_4 | 300 | 306 | PF00069 | 0.490 |
MOD_ProDKin_1 | 127 | 133 | PF00069 | 0.675 |
MOD_ProDKin_1 | 162 | 168 | PF00069 | 0.717 |
MOD_ProDKin_1 | 214 | 220 | PF00069 | 0.564 |
MOD_ProDKin_1 | 233 | 239 | PF00069 | 0.667 |
MOD_ProDKin_1 | 273 | 279 | PF00069 | 0.640 |
MOD_ProDKin_1 | 351 | 357 | PF00069 | 0.762 |
MOD_ProDKin_1 | 362 | 368 | PF00069 | 0.776 |
MOD_ProDKin_1 | 369 | 375 | PF00069 | 0.618 |
MOD_ProDKin_1 | 79 | 85 | PF00069 | 0.624 |
TRG_ENDOCYTIC_2 | 298 | 301 | PF00928 | 0.478 |
TRG_ER_diArg_1 | 397 | 400 | PF00400 | 0.683 |
TRG_NLS_MonoCore_2 | 3 | 8 | PF00514 | 0.637 |
TRG_NLS_MonoExtC_3 | 9 | 14 | PF00514 | 0.615 |
TRG_NLS_MonoExtN_4 | 4 | 9 | PF00514 | 0.675 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBY1 | Leptomonas seymouri | 33% | 100% |
A0A3Q8I8Z9 | Leishmania donovani | 99% | 100% |
A4H6F1 | Leishmania braziliensis | 64% | 98% |
E9ANI0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 76% | 99% |
Q4QH46 | Leishmania major | 80% | 100% |