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: E9B3D5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 176 | 180 | PF00656 | 0.631 |
CLV_C14_Caspase3-7 | 378 | 382 | PF00656 | 0.794 |
CLV_C14_Caspase3-7 | 98 | 102 | PF00656 | 0.539 |
CLV_NRD_NRD_1 | 210 | 212 | PF00675 | 0.515 |
CLV_NRD_NRD_1 | 355 | 357 | PF00675 | 0.734 |
CLV_NRD_NRD_1 | 368 | 370 | PF00675 | 0.624 |
CLV_NRD_NRD_1 | 404 | 406 | PF00675 | 0.776 |
CLV_NRD_NRD_1 | 58 | 60 | PF00675 | 0.597 |
CLV_NRD_NRD_1 | 79 | 81 | PF00675 | 0.521 |
CLV_PCSK_FUR_1 | 402 | 406 | PF00082 | 0.606 |
CLV_PCSK_KEX2_1 | 353 | 355 | PF00082 | 0.725 |
CLV_PCSK_KEX2_1 | 367 | 369 | PF00082 | 0.606 |
CLV_PCSK_KEX2_1 | 402 | 404 | PF00082 | 0.774 |
CLV_PCSK_KEX2_1 | 409 | 411 | PF00082 | 0.701 |
CLV_PCSK_KEX2_1 | 413 | 415 | PF00082 | 0.638 |
CLV_PCSK_KEX2_1 | 58 | 60 | PF00082 | 0.618 |
CLV_PCSK_KEX2_1 | 73 | 75 | PF00082 | 0.626 |
CLV_PCSK_PC1ET2_1 | 353 | 355 | PF00082 | 0.537 |
CLV_PCSK_PC1ET2_1 | 409 | 411 | PF00082 | 0.767 |
CLV_PCSK_PC1ET2_1 | 413 | 415 | PF00082 | 0.766 |
CLV_PCSK_PC1ET2_1 | 73 | 75 | PF00082 | 0.722 |
CLV_PCSK_PC7_1 | 363 | 369 | PF00082 | 0.640 |
CLV_PCSK_PC7_1 | 405 | 411 | PF00082 | 0.527 |
CLV_PCSK_SKI1_1 | 172 | 176 | PF00082 | 0.686 |
CLV_PCSK_SKI1_1 | 414 | 418 | PF00082 | 0.722 |
CLV_PCSK_SKI1_1 | 59 | 63 | PF00082 | 0.621 |
DEG_APCC_DBOX_1 | 273 | 281 | PF00400 | 0.537 |
DEG_MDM2_SWIB_1 | 220 | 228 | PF02201 | 0.673 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.749 |
DEG_SCF_TRCP1_1 | 65 | 70 | PF00400 | 0.473 |
DOC_ANK_TNKS_1 | 355 | 362 | PF00023 | 0.527 |
DOC_CYCLIN_RxL_1 | 56 | 66 | PF00134 | 0.566 |
DOC_MAPK_gen_1 | 271 | 279 | PF00069 | 0.540 |
DOC_MAPK_MEF2A_6 | 165 | 173 | PF00069 | 0.597 |
DOC_USP7_MATH_1 | 123 | 127 | PF00917 | 0.617 |
DOC_USP7_MATH_1 | 155 | 159 | PF00917 | 0.630 |
DOC_USP7_MATH_1 | 187 | 191 | PF00917 | 0.709 |
DOC_USP7_MATH_1 | 192 | 196 | PF00917 | 0.770 |
DOC_USP7_MATH_1 | 201 | 205 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 233 | 237 | PF00917 | 0.591 |
DOC_USP7_MATH_1 | 348 | 352 | PF00917 | 0.714 |
DOC_USP7_MATH_1 | 69 | 73 | PF00917 | 0.585 |
DOC_USP7_UBL2_3 | 409 | 413 | PF12436 | 0.738 |
DOC_WW_Pin1_4 | 190 | 195 | PF00397 | 0.738 |
DOC_WW_Pin1_4 | 344 | 349 | PF00397 | 0.638 |
DOC_WW_Pin1_4 | 384 | 389 | PF00397 | 0.747 |
DOC_WW_Pin1_4 | 96 | 101 | PF00397 | 0.604 |
LIG_14-3-3_CanoR_1 | 122 | 132 | PF00244 | 0.689 |
LIG_14-3-3_CanoR_1 | 274 | 280 | PF00244 | 0.732 |
LIG_14-3-3_CanoR_1 | 438 | 443 | PF00244 | 0.671 |
LIG_14-3-3_CanoR_1 | 68 | 75 | PF00244 | 0.667 |
LIG_Actin_WH2_2 | 156 | 174 | PF00022 | 0.680 |
LIG_FHA_1 | 155 | 161 | PF00498 | 0.644 |
LIG_FHA_1 | 173 | 179 | PF00498 | 0.616 |
LIG_FHA_1 | 2 | 8 | PF00498 | 0.558 |
LIG_FHA_1 | 220 | 226 | PF00498 | 0.431 |
LIG_FHA_2 | 148 | 154 | PF00498 | 0.590 |
LIG_FHA_2 | 35 | 41 | PF00498 | 0.470 |
LIG_FHA_2 | 88 | 94 | PF00498 | 0.793 |
LIG_FHA_2 | 96 | 102 | PF00498 | 0.693 |
LIG_GBD_Chelix_1 | 206 | 214 | PF00786 | 0.672 |
LIG_GBD_Chelix_1 | 53 | 61 | PF00786 | 0.702 |
LIG_LIR_Gen_1 | 222 | 232 | PF02991 | 0.614 |
LIG_LIR_Nem_3 | 222 | 227 | PF02991 | 0.623 |
LIG_PDZ_Class_1 | 438 | 443 | PF00595 | 0.668 |
LIG_Pex14_1 | 213 | 217 | PF04695 | 0.665 |
LIG_Pex14_2 | 217 | 221 | PF04695 | 0.690 |
LIG_SH2_SRC | 370 | 373 | PF00017 | 0.528 |
LIG_SH2_STAP1 | 299 | 303 | PF00017 | 0.613 |
LIG_SH2_STAT3 | 298 | 301 | PF00017 | 0.693 |
LIG_SH2_STAT5 | 216 | 219 | PF00017 | 0.673 |
LIG_SH2_STAT5 | 370 | 373 | PF00017 | 0.537 |
LIG_SH2_STAT5 | 75 | 78 | PF00017 | 0.615 |
LIG_SH3_3 | 138 | 144 | PF00018 | 0.730 |
LIG_SH3_3 | 188 | 194 | PF00018 | 0.637 |
LIG_SH3_3 | 270 | 276 | PF00018 | 0.540 |
LIG_SH3_3 | 79 | 85 | PF00018 | 0.608 |
LIG_Sin3_3 | 129 | 136 | PF02671 | 0.476 |
LIG_SUMO_SIM_par_1 | 429 | 435 | PF11976 | 0.645 |
LIG_TRAF2_1 | 18 | 21 | PF00917 | 0.691 |
LIG_UBA3_1 | 45 | 52 | PF00899 | 0.546 |
LIG_WW_3 | 271 | 275 | PF00397 | 0.537 |
MOD_CK1_1 | 190 | 196 | PF00069 | 0.715 |
MOD_CK1_1 | 231 | 237 | PF00069 | 0.658 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.714 |
MOD_CK1_1 | 344 | 350 | PF00069 | 0.594 |
MOD_CK1_1 | 374 | 380 | PF00069 | 0.786 |
MOD_CK1_1 | 382 | 388 | PF00069 | 0.608 |
MOD_CK1_1 | 87 | 93 | PF00069 | 0.734 |
MOD_CK2_1 | 15 | 21 | PF00069 | 0.684 |
MOD_CK2_1 | 332 | 338 | PF00069 | 0.626 |
MOD_CK2_1 | 34 | 40 | PF00069 | 0.455 |
MOD_CK2_1 | 384 | 390 | PF00069 | 0.521 |
MOD_GlcNHglycan | 126 | 129 | PF01048 | 0.508 |
MOD_GlcNHglycan | 156 | 160 | PF01048 | 0.711 |
MOD_GlcNHglycan | 197 | 200 | PF01048 | 0.579 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.581 |
MOD_GlcNHglycan | 334 | 337 | PF01048 | 0.545 |
MOD_GlcNHglycan | 350 | 353 | PF01048 | 0.783 |
MOD_GlcNHglycan | 377 | 380 | PF01048 | 0.633 |
MOD_GlcNHglycan | 418 | 422 | PF01048 | 0.606 |
MOD_GlcNHglycan | 64 | 68 | PF01048 | 0.726 |
MOD_GlcNHglycan | 86 | 89 | PF01048 | 0.802 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.641 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.725 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.602 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.680 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.711 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.567 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.796 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.635 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.657 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.771 |
MOD_N-GLC_2 | 312 | 314 | PF02516 | 0.488 |
MOD_NEK2_1 | 173 | 178 | PF00069 | 0.691 |
MOD_NEK2_1 | 206 | 211 | PF00069 | 0.553 |
MOD_NEK2_1 | 227 | 232 | PF00069 | 0.705 |
MOD_NEK2_1 | 329 | 334 | PF00069 | 0.741 |
MOD_NEK2_1 | 417 | 422 | PF00069 | 0.532 |
MOD_NEK2_1 | 63 | 68 | PF00069 | 0.652 |
MOD_PIKK_1 | 101 | 107 | PF00454 | 0.815 |
MOD_PIKK_1 | 330 | 336 | PF00454 | 0.737 |
MOD_PKA_1 | 73 | 79 | PF00069 | 0.715 |
MOD_PKA_2 | 228 | 234 | PF00069 | 0.541 |
MOD_PKA_2 | 375 | 381 | PF00069 | 0.596 |
MOD_PKA_2 | 67 | 73 | PF00069 | 0.682 |
MOD_Plk_1 | 155 | 161 | PF00069 | 0.714 |
MOD_Plk_1 | 380 | 386 | PF00069 | 0.586 |
MOD_Plk_4 | 275 | 281 | PF00069 | 0.709 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.644 |
MOD_ProDKin_1 | 190 | 196 | PF00069 | 0.739 |
MOD_ProDKin_1 | 344 | 350 | PF00069 | 0.639 |
MOD_ProDKin_1 | 384 | 390 | PF00069 | 0.746 |
MOD_ProDKin_1 | 96 | 102 | PF00069 | 0.605 |
TRG_ENDOCYTIC_2 | 216 | 219 | PF00928 | 0.601 |
TRG_ER_diArg_1 | 119 | 122 | PF00400 | 0.740 |
TRG_ER_diArg_1 | 354 | 356 | PF00400 | 0.730 |
TRG_ER_diArg_1 | 367 | 369 | PF00400 | 0.665 |
TRG_ER_diArg_1 | 402 | 405 | PF00400 | 0.712 |
TRG_ER_diArg_1 | 437 | 440 | PF00400 | 0.730 |
TRG_ER_diArg_1 | 57 | 59 | PF00400 | 0.535 |
TRG_Pf-PMV_PEXEL_1 | 59 | 64 | PF00026 | 0.593 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S5H7T2 | Leishmania donovani | 80% | 100% |
A4HKZ5 | Leishmania braziliensis | 57% | 100% |
A4I8H5 | Leishmania infantum | 80% | 100% |
Q4Q4R7 | Leishmania major | 80% | 100% |