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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: Q4Q7K7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 106 | 110 | PF00656 | 0.585 |
CLV_NRD_NRD_1 | 192 | 194 | PF00675 | 0.803 |
CLV_NRD_NRD_1 | 198 | 200 | PF00675 | 0.815 |
CLV_NRD_NRD_1 | 67 | 69 | PF00675 | 0.712 |
CLV_NRD_NRD_1 | 91 | 93 | PF00675 | 0.617 |
CLV_PCSK_KEX2_1 | 192 | 194 | PF00082 | 0.762 |
CLV_PCSK_KEX2_1 | 198 | 200 | PF00082 | 0.786 |
CLV_PCSK_KEX2_1 | 45 | 47 | PF00082 | 0.706 |
CLV_PCSK_KEX2_1 | 91 | 93 | PF00082 | 0.617 |
CLV_PCSK_PC1ET2_1 | 45 | 47 | PF00082 | 0.706 |
CLV_PCSK_SKI1_1 | 135 | 139 | PF00082 | 0.538 |
CLV_PCSK_SKI1_1 | 396 | 400 | PF00082 | 0.542 |
CLV_PCSK_SKI1_1 | 446 | 450 | PF00082 | 0.592 |
CLV_PCSK_SKI1_1 | 69 | 73 | PF00082 | 0.596 |
DOC_CDC14_PxL_1 | 267 | 275 | PF14671 | 0.633 |
DOC_CKS1_1 | 241 | 246 | PF01111 | 0.576 |
DOC_CKS1_1 | 77 | 82 | PF01111 | 0.663 |
DOC_CYCLIN_yClb1_LxF_4 | 399 | 405 | PF00134 | 0.545 |
DOC_CYCLIN_yCln2_LP_2 | 151 | 157 | PF00134 | 0.632 |
DOC_CYCLIN_yCln2_LP_2 | 349 | 355 | PF00134 | 0.608 |
DOC_PP2B_LxvP_1 | 151 | 154 | PF13499 | 0.646 |
DOC_PP4_FxxP_1 | 404 | 407 | PF00568 | 0.555 |
DOC_PP4_FxxP_1 | 410 | 413 | PF00568 | 0.524 |
DOC_PP4_MxPP_1 | 78 | 81 | PF00568 | 0.529 |
DOC_USP7_MATH_1 | 157 | 161 | PF00917 | 0.619 |
DOC_USP7_MATH_1 | 170 | 174 | PF00917 | 0.642 |
DOC_USP7_MATH_1 | 307 | 311 | PF00917 | 0.636 |
DOC_USP7_MATH_1 | 379 | 383 | PF00917 | 0.485 |
DOC_WW_Pin1_4 | 116 | 121 | PF00397 | 0.584 |
DOC_WW_Pin1_4 | 153 | 158 | PF00397 | 0.642 |
DOC_WW_Pin1_4 | 240 | 245 | PF00397 | 0.644 |
DOC_WW_Pin1_4 | 274 | 279 | PF00397 | 0.664 |
DOC_WW_Pin1_4 | 327 | 332 | PF00397 | 0.688 |
DOC_WW_Pin1_4 | 359 | 364 | PF00397 | 0.634 |
DOC_WW_Pin1_4 | 375 | 380 | PF00397 | 0.470 |
DOC_WW_Pin1_4 | 6 | 11 | PF00397 | 0.636 |
DOC_WW_Pin1_4 | 76 | 81 | PF00397 | 0.656 |
LIG_14-3-3_CanoR_1 | 161 | 168 | PF00244 | 0.704 |
LIG_14-3-3_CanoR_1 | 300 | 305 | PF00244 | 0.634 |
LIG_14-3-3_CanoR_1 | 361 | 367 | PF00244 | 0.611 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.566 |
LIG_BIR_III_4 | 217 | 221 | PF00653 | 0.580 |
LIG_Clathr_ClatBox_1 | 402 | 406 | PF01394 | 0.547 |
LIG_CtBP_PxDLS_1 | 48 | 52 | PF00389 | 0.654 |
LIG_FHA_1 | 178 | 184 | PF00498 | 0.762 |
LIG_FHA_1 | 283 | 289 | PF00498 | 0.609 |
LIG_FHA_1 | 397 | 403 | PF00498 | 0.538 |
LIG_FHA_2 | 104 | 110 | PF00498 | 0.651 |
LIG_FHA_2 | 260 | 266 | PF00498 | 0.632 |
LIG_FHA_2 | 424 | 430 | PF00498 | 0.549 |
LIG_FHA_2 | 62 | 68 | PF00498 | 0.596 |
LIG_HCF-1_HBM_1 | 420 | 423 | PF13415 | 0.564 |
LIG_LIR_Apic_2 | 74 | 80 | PF02991 | 0.653 |
LIG_LIR_Gen_1 | 256 | 266 | PF02991 | 0.742 |
LIG_LIR_Nem_3 | 256 | 261 | PF02991 | 0.757 |
LIG_LIR_Nem_3 | 262 | 267 | PF02991 | 0.628 |
LIG_PDZ_Class_1 | 446 | 451 | PF00595 | 0.600 |
LIG_Pex14_2 | 394 | 398 | PF04695 | 0.543 |
LIG_SH2_CRK | 77 | 81 | PF00017 | 0.596 |
LIG_SH3_1 | 275 | 281 | PF00018 | 0.671 |
LIG_SH3_3 | 109 | 115 | PF00018 | 0.581 |
LIG_SH3_3 | 151 | 157 | PF00018 | 0.632 |
LIG_SH3_3 | 238 | 244 | PF00018 | 0.815 |
LIG_SH3_3 | 266 | 272 | PF00018 | 0.617 |
LIG_SH3_3 | 275 | 281 | PF00018 | 0.587 |
LIG_SH3_3 | 29 | 35 | PF00018 | 0.643 |
LIG_SH3_3 | 349 | 355 | PF00018 | 0.652 |
LIG_SH3_3 | 402 | 408 | PF00018 | 0.549 |
LIG_SH3_3 | 7 | 13 | PF00018 | 0.635 |
LIG_SUMO_SIM_par_1 | 412 | 417 | PF11976 | 0.576 |
LIG_TRAF2_1 | 143 | 146 | PF00917 | 0.600 |
LIG_TRAF2_1 | 338 | 341 | PF00917 | 0.644 |
LIG_TRAF2_1 | 435 | 438 | PF00917 | 0.579 |
LIG_WW_3 | 58 | 62 | PF00397 | 0.617 |
LIG_WW_3 | 79 | 83 | PF00397 | 0.537 |
MOD_CDK_SPK_2 | 274 | 279 | PF00069 | 0.664 |
MOD_CDK_SPxK_1 | 76 | 82 | PF00069 | 0.660 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.604 |
MOD_CK1_1 | 160 | 166 | PF00069 | 0.643 |
MOD_CK1_1 | 234 | 240 | PF00069 | 0.597 |
MOD_CK1_1 | 253 | 259 | PF00069 | 0.526 |
MOD_CK1_1 | 282 | 288 | PF00069 | 0.635 |
MOD_CK1_1 | 318 | 324 | PF00069 | 0.665 |
MOD_CK1_1 | 330 | 336 | PF00069 | 0.664 |
MOD_CK1_1 | 357 | 363 | PF00069 | 0.611 |
MOD_CK1_1 | 390 | 396 | PF00069 | 0.510 |
MOD_CK2_1 | 140 | 146 | PF00069 | 0.614 |
MOD_CK2_1 | 153 | 159 | PF00069 | 0.547 |
MOD_CK2_1 | 318 | 324 | PF00069 | 0.674 |
MOD_CK2_1 | 432 | 438 | PF00069 | 0.582 |
MOD_CK2_1 | 61 | 67 | PF00069 | 0.601 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.714 |
MOD_GlcNHglycan | 19 | 23 | PF01048 | 0.681 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.594 |
MOD_GlcNHglycan | 387 | 392 | PF01048 | 0.529 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.625 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.615 |
MOD_GSK3_1 | 153 | 160 | PF00069 | 0.558 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.576 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.626 |
MOD_GSK3_1 | 250 | 257 | PF00069 | 0.542 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.631 |
MOD_GSK3_1 | 326 | 333 | PF00069 | 0.783 |
MOD_GSK3_1 | 353 | 360 | PF00069 | 0.599 |
MOD_GSK3_1 | 361 | 368 | PF00069 | 0.529 |
MOD_GSK3_1 | 375 | 382 | PF00069 | 0.470 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.685 |
MOD_N-GLC_1 | 107 | 112 | PF02516 | 0.652 |
MOD_N-GLC_1 | 298 | 303 | PF02516 | 0.561 |
MOD_NEK2_1 | 18 | 23 | PF00069 | 0.690 |
MOD_NEK2_1 | 273 | 278 | PF00069 | 0.734 |
MOD_NEK2_1 | 298 | 303 | PF00069 | 0.578 |
MOD_NEK2_1 | 30 | 35 | PF00069 | 0.611 |
MOD_NEK2_1 | 326 | 331 | PF00069 | 0.715 |
MOD_NEK2_1 | 54 | 59 | PF00069 | 0.591 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.636 |
MOD_NEK2_1 | 96 | 101 | PF00069 | 0.748 |
MOD_NEK2_2 | 20 | 25 | PF00069 | 0.569 |
MOD_NEK2_2 | 379 | 384 | PF00069 | 0.484 |
MOD_PIKK_1 | 203 | 209 | PF00454 | 0.688 |
MOD_PIKK_1 | 282 | 288 | PF00454 | 0.635 |
MOD_PIKK_1 | 54 | 60 | PF00454 | 0.656 |
MOD_PKA_2 | 160 | 166 | PF00069 | 0.709 |
MOD_PKA_2 | 181 | 187 | PF00069 | 0.624 |
MOD_PKA_2 | 299 | 305 | PF00069 | 0.625 |
MOD_Plk_1 | 107 | 113 | PF00069 | 0.653 |
MOD_Plk_1 | 250 | 256 | PF00069 | 0.640 |
MOD_Plk_1 | 379 | 385 | PF00069 | 0.483 |
MOD_Plk_2-3 | 432 | 438 | PF00069 | 0.582 |
MOD_Plk_4 | 107 | 113 | PF00069 | 0.631 |
MOD_Plk_4 | 279 | 285 | PF00069 | 0.678 |
MOD_Plk_4 | 423 | 429 | PF00069 | 0.549 |
MOD_ProDKin_1 | 116 | 122 | PF00069 | 0.584 |
MOD_ProDKin_1 | 153 | 159 | PF00069 | 0.646 |
MOD_ProDKin_1 | 240 | 246 | PF00069 | 0.643 |
MOD_ProDKin_1 | 274 | 280 | PF00069 | 0.667 |
MOD_ProDKin_1 | 327 | 333 | PF00069 | 0.689 |
MOD_ProDKin_1 | 359 | 365 | PF00069 | 0.634 |
MOD_ProDKin_1 | 375 | 381 | PF00069 | 0.469 |
MOD_ProDKin_1 | 6 | 12 | PF00069 | 0.637 |
MOD_ProDKin_1 | 76 | 82 | PF00069 | 0.660 |
MOD_SUMO_rev_2 | 437 | 445 | PF00179 | 0.568 |
MOD_SUMO_rev_2 | 63 | 71 | PF00179 | 0.653 |
TRG_DiLeu_BaEn_3 | 49 | 55 | PF01217 | 0.575 |
TRG_DiLeu_BaLyEn_6 | 112 | 117 | PF01217 | 0.632 |
TRG_DiLeu_BaLyEn_6 | 269 | 274 | PF01217 | 0.637 |
TRG_ER_diArg_1 | 191 | 193 | PF00400 | 0.684 |
TRG_Pf-PMV_PEXEL_1 | 45 | 49 | PF00026 | 0.655 |
TRG_Pf-PMV_PEXEL_1 | 82 | 87 | PF00026 | 0.585 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IRU8 | Leishmania donovani | 84% | 77% |
A4HI51 | Leishmania braziliensis | 63% | 100% |
A4I5C7 | Leishmania infantum | 84% | 100% |
E9B0M5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |