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: A0A3Q8IEK2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 121 | 125 | PF00656 | 0.777 |
CLV_C14_Caspase3-7 | 127 | 131 | PF00656 | 0.750 |
CLV_C14_Caspase3-7 | 178 | 182 | PF00656 | 0.837 |
CLV_C14_Caspase3-7 | 187 | 191 | PF00656 | 0.680 |
CLV_C14_Caspase3-7 | 206 | 210 | PF00656 | 0.740 |
CLV_NRD_NRD_1 | 115 | 117 | PF00675 | 0.517 |
CLV_NRD_NRD_1 | 196 | 198 | PF00675 | 0.768 |
CLV_NRD_NRD_1 | 199 | 201 | PF00675 | 0.634 |
CLV_NRD_NRD_1 | 33 | 35 | PF00675 | 0.814 |
CLV_NRD_NRD_1 | 443 | 445 | PF00675 | 0.503 |
CLV_NRD_NRD_1 | 446 | 448 | PF00675 | 0.473 |
CLV_NRD_NRD_1 | 99 | 101 | PF00675 | 0.738 |
CLV_PCSK_FUR_1 | 197 | 201 | PF00082 | 0.804 |
CLV_PCSK_FUR_1 | 441 | 445 | PF00082 | 0.430 |
CLV_PCSK_KEX2_1 | 101 | 103 | PF00082 | 0.695 |
CLV_PCSK_KEX2_1 | 115 | 117 | PF00082 | 0.549 |
CLV_PCSK_KEX2_1 | 164 | 166 | PF00082 | 0.688 |
CLV_PCSK_KEX2_1 | 196 | 198 | PF00082 | 0.762 |
CLV_PCSK_KEX2_1 | 199 | 201 | PF00082 | 0.630 |
CLV_PCSK_KEX2_1 | 33 | 35 | PF00082 | 0.814 |
CLV_PCSK_KEX2_1 | 443 | 445 | PF00082 | 0.496 |
CLV_PCSK_KEX2_1 | 446 | 448 | PF00082 | 0.481 |
CLV_PCSK_KEX2_1 | 86 | 88 | PF00082 | 0.790 |
CLV_PCSK_PC1ET2_1 | 101 | 103 | PF00082 | 0.802 |
CLV_PCSK_PC1ET2_1 | 164 | 166 | PF00082 | 0.633 |
CLV_PCSK_PC1ET2_1 | 86 | 88 | PF00082 | 0.738 |
CLV_PCSK_PC7_1 | 111 | 117 | PF00082 | 0.777 |
CLV_PCSK_SKI1_1 | 282 | 286 | PF00082 | 0.484 |
CLV_PCSK_SKI1_1 | 297 | 301 | PF00082 | 0.335 |
CLV_PCSK_SKI1_1 | 456 | 460 | PF00082 | 0.725 |
DEG_APCC_DBOX_1 | 318 | 326 | PF00400 | 0.411 |
DEG_APCC_DBOX_1 | 445 | 453 | PF00400 | 0.436 |
DEG_SPOP_SBC_1 | 217 | 221 | PF00917 | 0.618 |
DOC_CYCLIN_RxL_1 | 240 | 251 | PF00134 | 0.640 |
DOC_MAPK_gen_1 | 317 | 325 | PF00069 | 0.513 |
DOC_MAPK_JIP1_4 | 319 | 325 | PF00069 | 0.411 |
DOC_PP1_RVXF_1 | 417 | 423 | PF00149 | 0.411 |
DOC_PP4_FxxP_1 | 140 | 143 | PF00568 | 0.829 |
DOC_PP4_FxxP_1 | 334 | 337 | PF00568 | 0.411 |
DOC_USP7_MATH_1 | 223 | 227 | PF00917 | 0.734 |
DOC_USP7_MATH_1 | 77 | 81 | PF00917 | 0.840 |
DOC_WW_Pin1_4 | 219 | 224 | PF00397 | 0.639 |
DOC_WW_Pin1_4 | 409 | 414 | PF00397 | 0.513 |
DOC_WW_Pin1_4 | 92 | 97 | PF00397 | 0.716 |
LIG_14-3-3_CanoR_1 | 100 | 106 | PF00244 | 0.748 |
LIG_14-3-3_CanoR_1 | 311 | 316 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 380 | 387 | PF00244 | 0.506 |
LIG_14-3-3_CanoR_1 | 444 | 450 | PF00244 | 0.471 |
LIG_14-3-3_CanoR_1 | 45 | 51 | PF00244 | 0.720 |
LIG_BRCT_BRCA1_1 | 136 | 140 | PF00533 | 0.849 |
LIG_BRCT_BRCA1_1 | 291 | 295 | PF00533 | 0.513 |
LIG_BRCT_BRCA1_1 | 62 | 66 | PF00533 | 0.705 |
LIG_deltaCOP1_diTrp_1 | 287 | 295 | PF00928 | 0.436 |
LIG_EH_1 | 331 | 335 | PF12763 | 0.411 |
LIG_FHA_1 | 203 | 209 | PF00498 | 0.775 |
LIG_FHA_1 | 231 | 237 | PF00498 | 0.603 |
LIG_FHA_1 | 310 | 316 | PF00498 | 0.641 |
LIG_FHA_1 | 457 | 463 | PF00498 | 0.739 |
LIG_FHA_2 | 149 | 155 | PF00498 | 0.768 |
LIG_FHA_2 | 176 | 182 | PF00498 | 0.837 |
LIG_LIR_Apic_2 | 137 | 143 | PF02991 | 0.836 |
LIG_LIR_Apic_2 | 347 | 353 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 397 | 401 | PF02991 | 0.378 |
LIG_MYND_1 | 333 | 337 | PF01753 | 0.411 |
LIG_SH2_NCK_1 | 256 | 260 | PF00017 | 0.411 |
LIG_SH2_STAP1 | 359 | 363 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 244 | 247 | PF00017 | 0.573 |
LIG_SH3_3 | 368 | 374 | PF00018 | 0.436 |
LIG_SH3_3 | 91 | 97 | PF00018 | 0.613 |
LIG_TRAF2_1 | 152 | 155 | PF00917 | 0.845 |
LIG_TRAF2_1 | 388 | 391 | PF00917 | 0.679 |
LIG_TRAF2_1 | 72 | 75 | PF00917 | 0.774 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.709 |
MOD_CK1_1 | 219 | 225 | PF00069 | 0.682 |
MOD_CK1_1 | 341 | 347 | PF00069 | 0.429 |
MOD_CK1_1 | 389 | 395 | PF00069 | 0.560 |
MOD_CK1_1 | 445 | 451 | PF00069 | 0.438 |
MOD_CK1_1 | 46 | 52 | PF00069 | 0.761 |
MOD_CK2_1 | 148 | 154 | PF00069 | 0.737 |
MOD_CK2_1 | 171 | 177 | PF00069 | 0.724 |
MOD_CK2_1 | 181 | 187 | PF00069 | 0.789 |
MOD_CK2_1 | 218 | 224 | PF00069 | 0.768 |
MOD_CK2_1 | 69 | 75 | PF00069 | 0.745 |
MOD_GlcNHglycan | 106 | 109 | PF01048 | 0.790 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.619 |
MOD_GlcNHglycan | 166 | 169 | PF01048 | 0.735 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.700 |
MOD_GlcNHglycan | 274 | 277 | PF01048 | 0.353 |
MOD_GlcNHglycan | 291 | 294 | PF01048 | 0.353 |
MOD_GlcNHglycan | 301 | 304 | PF01048 | 0.348 |
MOD_GlcNHglycan | 338 | 343 | PF01048 | 0.336 |
MOD_GlcNHglycan | 382 | 385 | PF01048 | 0.586 |
MOD_GlcNHglycan | 40 | 43 | PF01048 | 0.788 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.767 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.846 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.800 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.743 |
MOD_GSK3_1 | 409 | 416 | PF00069 | 0.513 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.797 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.777 |
MOD_LATS_1 | 454 | 460 | PF00433 | 0.711 |
MOD_N-GLC_1 | 309 | 314 | PF02516 | 0.620 |
MOD_N-GLC_2 | 91 | 93 | PF02516 | 0.663 |
MOD_NEK2_1 | 203 | 208 | PF00069 | 0.685 |
MOD_NEK2_1 | 272 | 277 | PF00069 | 0.513 |
MOD_NEK2_1 | 378 | 383 | PF00069 | 0.507 |
MOD_NEK2_1 | 60 | 65 | PF00069 | 0.768 |
MOD_PIKK_1 | 181 | 187 | PF00454 | 0.838 |
MOD_PIKK_1 | 378 | 384 | PF00454 | 0.673 |
MOD_PIKK_1 | 70 | 76 | PF00454 | 0.795 |
MOD_PKA_1 | 101 | 107 | PF00069 | 0.744 |
MOD_PKA_1 | 164 | 170 | PF00069 | 0.676 |
MOD_PKA_2 | 101 | 107 | PF00069 | 0.748 |
MOD_PKA_2 | 110 | 116 | PF00069 | 0.741 |
MOD_PKA_2 | 164 | 170 | PF00069 | 0.741 |
MOD_PKA_2 | 310 | 316 | PF00069 | 0.539 |
MOD_PKA_2 | 344 | 350 | PF00069 | 0.375 |
MOD_PKA_2 | 355 | 361 | PF00069 | 0.453 |
MOD_PKA_2 | 442 | 448 | PF00069 | 0.419 |
MOD_PKA_2 | 68 | 74 | PF00069 | 0.752 |
MOD_Plk_1 | 129 | 135 | PF00069 | 0.550 |
MOD_Plk_1 | 389 | 395 | PF00069 | 0.662 |
MOD_Plk_1 | 431 | 437 | PF00069 | 0.411 |
MOD_Plk_1 | 60 | 66 | PF00069 | 0.642 |
MOD_Plk_2-3 | 142 | 148 | PF00069 | 0.817 |
MOD_Plk_4 | 203 | 209 | PF00069 | 0.585 |
MOD_Plk_4 | 344 | 350 | PF00069 | 0.355 |
MOD_Plk_4 | 389 | 395 | PF00069 | 0.640 |
MOD_ProDKin_1 | 219 | 225 | PF00069 | 0.639 |
MOD_ProDKin_1 | 409 | 415 | PF00069 | 0.513 |
MOD_ProDKin_1 | 92 | 98 | PF00069 | 0.715 |
MOD_SUMO_for_1 | 16 | 19 | PF00179 | 0.636 |
MOD_SUMO_for_1 | 163 | 166 | PF00179 | 0.620 |
MOD_SUMO_for_1 | 335 | 338 | PF00179 | 0.402 |
MOD_SUMO_rev_2 | 409 | 418 | PF00179 | 0.389 |
MOD_SUMO_rev_2 | 79 | 88 | PF00179 | 0.812 |
TRG_DiLeu_BaEn_4 | 390 | 396 | PF01217 | 0.661 |
TRG_ENDOCYTIC_2 | 244 | 247 | PF00928 | 0.615 |
TRG_ER_diArg_1 | 115 | 117 | PF00400 | 0.746 |
TRG_ER_diArg_1 | 196 | 199 | PF00400 | 0.760 |
TRG_ER_diArg_1 | 442 | 444 | PF00400 | 0.506 |
TRG_NLS_Bipartite_1 | 86 | 104 | PF00514 | 0.807 |
TRG_NLS_MonoExtN_4 | 97 | 104 | PF00514 | 0.660 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IKX8 | Leptomonas seymouri | 52% | 98% |
A4HHL8 | Leishmania braziliensis | 73% | 100% |
A4I4S7 | Leishmania infantum | 99% | 100% |
E9AE80 | Leishmania major | 89% | 100% |
E9ALK5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |