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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: E9B464
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 177 | 181 | PF00656 | 0.495 |
CLV_C14_Caspase3-7 | 395 | 399 | PF00656 | 0.694 |
CLV_C14_Caspase3-7 | 425 | 429 | PF00656 | 0.697 |
CLV_NRD_NRD_1 | 127 | 129 | PF00675 | 0.545 |
CLV_NRD_NRD_1 | 378 | 380 | PF00675 | 0.531 |
CLV_PCSK_KEX2_1 | 118 | 120 | PF00082 | 0.576 |
CLV_PCSK_KEX2_1 | 306 | 308 | PF00082 | 0.700 |
CLV_PCSK_KEX2_1 | 320 | 322 | PF00082 | 0.657 |
CLV_PCSK_KEX2_1 | 378 | 380 | PF00082 | 0.531 |
CLV_PCSK_KEX2_1 | 440 | 442 | PF00082 | 0.599 |
CLV_PCSK_PC1ET2_1 | 118 | 120 | PF00082 | 0.659 |
CLV_PCSK_PC1ET2_1 | 306 | 308 | PF00082 | 0.700 |
CLV_PCSK_PC1ET2_1 | 320 | 322 | PF00082 | 0.657 |
CLV_PCSK_PC1ET2_1 | 440 | 442 | PF00082 | 0.650 |
CLV_PCSK_SKI1_1 | 138 | 142 | PF00082 | 0.609 |
CLV_PCSK_SKI1_1 | 19 | 23 | PF00082 | 0.549 |
CLV_PCSK_SKI1_1 | 229 | 233 | PF00082 | 0.418 |
CLV_PCSK_SKI1_1 | 309 | 313 | PF00082 | 0.725 |
CLV_PCSK_SKI1_1 | 378 | 382 | PF00082 | 0.526 |
CLV_PCSK_SKI1_1 | 407 | 411 | PF00082 | 0.600 |
DEG_APCC_DBOX_1 | 214 | 222 | PF00400 | 0.563 |
DEG_APCC_DBOX_1 | 228 | 236 | PF00400 | 0.430 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.543 |
DEG_SPOP_SBC_1 | 368 | 372 | PF00917 | 0.640 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 417 | 424 | PF00134 | 0.371 |
DOC_MAPK_HePTP_8 | 318 | 330 | PF00069 | 0.602 |
DOC_MAPK_MEF2A_6 | 321 | 330 | PF00069 | 0.596 |
DOC_PP2B_LxvP_1 | 427 | 430 | PF13499 | 0.637 |
DOC_SPAK_OSR1_1 | 247 | 251 | PF12202 | 0.484 |
DOC_USP7_MATH_1 | 14 | 18 | PF00917 | 0.480 |
DOC_USP7_MATH_1 | 172 | 176 | PF00917 | 0.788 |
DOC_USP7_MATH_1 | 202 | 206 | PF00917 | 0.667 |
DOC_USP7_MATH_1 | 256 | 260 | PF00917 | 0.496 |
DOC_USP7_MATH_1 | 341 | 345 | PF00917 | 0.799 |
DOC_USP7_MATH_1 | 364 | 368 | PF00917 | 0.737 |
DOC_USP7_MATH_1 | 374 | 378 | PF00917 | 0.618 |
DOC_USP7_MATH_1 | 63 | 67 | PF00917 | 0.631 |
DOC_USP7_MATH_1 | 74 | 78 | PF00917 | 0.709 |
DOC_WW_Pin1_4 | 166 | 171 | PF00397 | 0.695 |
DOC_WW_Pin1_4 | 183 | 188 | PF00397 | 0.434 |
DOC_WW_Pin1_4 | 400 | 405 | PF00397 | 0.766 |
LIG_14-3-3_CanoR_1 | 111 | 117 | PF00244 | 0.503 |
LIG_14-3-3_CanoR_1 | 173 | 183 | PF00244 | 0.743 |
LIG_14-3-3_CanoR_1 | 19 | 24 | PF00244 | 0.497 |
LIG_14-3-3_CanoR_1 | 215 | 219 | PF00244 | 0.595 |
LIG_14-3-3_CanoR_1 | 234 | 242 | PF00244 | 0.560 |
LIG_14-3-3_CanoR_1 | 331 | 337 | PF00244 | 0.708 |
LIG_14-3-3_CanoR_1 | 378 | 383 | PF00244 | 0.633 |
LIG_14-3-3_CanoR_1 | 44 | 52 | PF00244 | 0.536 |
LIG_14-3-3_CanoR_1 | 441 | 450 | PF00244 | 0.465 |
LIG_BRCT_BRCA1_1 | 204 | 208 | PF00533 | 0.703 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.503 |
LIG_FHA_1 | 149 | 155 | PF00498 | 0.578 |
LIG_FHA_1 | 284 | 290 | PF00498 | 0.801 |
LIG_FHA_1 | 30 | 36 | PF00498 | 0.498 |
LIG_FHA_1 | 353 | 359 | PF00498 | 0.734 |
LIG_FHA_2 | 28 | 34 | PF00498 | 0.542 |
LIG_FHA_2 | 379 | 385 | PF00498 | 0.734 |
LIG_LIR_Gen_1 | 108 | 116 | PF02991 | 0.453 |
LIG_LIR_Gen_1 | 17 | 26 | PF02991 | 0.494 |
LIG_LIR_Gen_1 | 236 | 244 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 108 | 112 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 17 | 23 | PF02991 | 0.488 |
LIG_MYND_1 | 70 | 74 | PF01753 | 0.717 |
LIG_SH2_CRK | 109 | 113 | PF00017 | 0.459 |
LIG_SH2_CRK | 7 | 11 | PF00017 | 0.450 |
LIG_SH2_NCK_1 | 255 | 259 | PF00017 | 0.535 |
LIG_SH2_STAT5 | 156 | 159 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 20 | 23 | PF00017 | 0.500 |
LIG_SH3_2 | 326 | 331 | PF14604 | 0.495 |
LIG_SH3_3 | 184 | 190 | PF00018 | 0.626 |
LIG_SH3_3 | 20 | 26 | PF00018 | 0.617 |
LIG_SH3_3 | 323 | 329 | PF00018 | 0.667 |
LIG_SH3_3 | 67 | 73 | PF00018 | 0.740 |
LIG_SUMO_SIM_par_1 | 112 | 117 | PF11976 | 0.498 |
LIG_TRAF2_1 | 237 | 240 | PF00917 | 0.501 |
LIG_TYR_ITIM | 5 | 10 | PF00017 | 0.442 |
LIG_UBA3_1 | 207 | 212 | PF00899 | 0.722 |
MOD_CDK_SPK_2 | 168 | 173 | PF00069 | 0.490 |
MOD_CDK_SPxxK_3 | 166 | 173 | PF00069 | 0.703 |
MOD_CDK_SPxxK_3 | 400 | 407 | PF00069 | 0.675 |
MOD_CK1_1 | 149 | 155 | PF00069 | 0.690 |
MOD_CK1_1 | 276 | 282 | PF00069 | 0.619 |
MOD_CK1_1 | 367 | 373 | PF00069 | 0.787 |
MOD_CK1_1 | 75 | 81 | PF00069 | 0.720 |
MOD_CK2_1 | 233 | 239 | PF00069 | 0.490 |
MOD_CK2_1 | 254 | 260 | PF00069 | 0.515 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.672 |
MOD_GlcNHglycan | 16 | 19 | PF01048 | 0.459 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.638 |
MOD_GlcNHglycan | 235 | 238 | PF01048 | 0.415 |
MOD_GlcNHglycan | 256 | 259 | PF01048 | 0.521 |
MOD_GlcNHglycan | 276 | 279 | PF01048 | 0.652 |
MOD_GlcNHglycan | 343 | 346 | PF01048 | 0.794 |
MOD_GlcNHglycan | 366 | 369 | PF01048 | 0.760 |
MOD_GlcNHglycan | 374 | 377 | PF01048 | 0.784 |
MOD_GlcNHglycan | 391 | 394 | PF01048 | 0.616 |
MOD_GlcNHglycan | 400 | 403 | PF01048 | 0.614 |
MOD_GlcNHglycan | 433 | 436 | PF01048 | 0.658 |
MOD_GlcNHglycan | 443 | 446 | PF01048 | 0.582 |
MOD_GlcNHglycan | 65 | 68 | PF01048 | 0.692 |
MOD_GlcNHglycan | 76 | 80 | PF01048 | 0.749 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.597 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.462 |
MOD_GSK3_1 | 168 | 175 | PF00069 | 0.528 |
MOD_GSK3_1 | 250 | 257 | PF00069 | 0.427 |
MOD_GSK3_1 | 276 | 283 | PF00069 | 0.641 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.719 |
MOD_GSK3_1 | 339 | 346 | PF00069 | 0.733 |
MOD_GSK3_1 | 363 | 370 | PF00069 | 0.705 |
MOD_GSK3_1 | 374 | 381 | PF00069 | 0.751 |
MOD_GSK3_1 | 385 | 392 | PF00069 | 0.798 |
MOD_GSK3_1 | 57 | 64 | PF00069 | 0.392 |
MOD_N-GLC_1 | 45 | 50 | PF02516 | 0.478 |
MOD_NEK2_1 | 112 | 117 | PF00069 | 0.453 |
MOD_NEK2_1 | 148 | 153 | PF00069 | 0.608 |
MOD_NEK2_1 | 182 | 187 | PF00069 | 0.551 |
MOD_NEK2_1 | 332 | 337 | PF00069 | 0.607 |
MOD_NEK2_1 | 82 | 87 | PF00069 | 0.778 |
MOD_OFUCOSY | 249 | 254 | PF10250 | 0.461 |
MOD_PIKK_1 | 202 | 208 | PF00454 | 0.620 |
MOD_PKA_1 | 378 | 384 | PF00069 | 0.522 |
MOD_PKA_2 | 110 | 116 | PF00069 | 0.497 |
MOD_PKA_2 | 172 | 178 | PF00069 | 0.767 |
MOD_PKA_2 | 214 | 220 | PF00069 | 0.743 |
MOD_PKA_2 | 233 | 239 | PF00069 | 0.497 |
MOD_PKA_2 | 378 | 384 | PF00069 | 0.649 |
MOD_Plk_1 | 299 | 305 | PF00069 | 0.735 |
MOD_Plk_1 | 45 | 51 | PF00069 | 0.534 |
MOD_Plk_4 | 290 | 296 | PF00069 | 0.700 |
MOD_Plk_4 | 314 | 320 | PF00069 | 0.601 |
MOD_Plk_4 | 422 | 428 | PF00069 | 0.616 |
MOD_ProDKin_1 | 166 | 172 | PF00069 | 0.695 |
MOD_ProDKin_1 | 183 | 189 | PF00069 | 0.430 |
MOD_ProDKin_1 | 400 | 406 | PF00069 | 0.758 |
MOD_SUMO_for_1 | 311 | 314 | PF00179 | 0.747 |
MOD_SUMO_rev_2 | 322 | 329 | PF00179 | 0.632 |
TRG_DiLeu_BaEn_1 | 53 | 58 | PF01217 | 0.522 |
TRG_DiLeu_BaLyEn_6 | 5 | 10 | PF01217 | 0.442 |
TRG_ENDOCYTIC_2 | 109 | 112 | PF00928 | 0.454 |
TRG_ENDOCYTIC_2 | 20 | 23 | PF00928 | 0.488 |
TRG_ENDOCYTIC_2 | 7 | 10 | PF00928 | 0.441 |
TRG_NES_CRM1_1 | 414 | 428 | PF08389 | 0.605 |
TRG_Pf-PMV_PEXEL_1 | 119 | 123 | PF00026 | 0.626 |
TRG_Pf-PMV_PEXEL_1 | 138 | 142 | PF00026 | 0.588 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1ILE8 | Leptomonas seymouri | 47% | 100% |
A0A3Q8IH00 | Leishmania donovani | 89% | 99% |
A4HLT8 | Leishmania braziliensis | 72% | 99% |
D0A688 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
E9AHP4 | Leishmania infantum | 89% | 99% |
Q4Q3W2 | Leishmania major | 88% | 100% |