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: E9ALK5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 127 | 131 | PF00656 | 0.690 |
CLV_C14_Caspase3-7 | 178 | 182 | PF00656 | 0.821 |
CLV_C14_Caspase3-7 | 187 | 191 | PF00656 | 0.675 |
CLV_NRD_NRD_1 | 115 | 117 | PF00675 | 0.793 |
CLV_NRD_NRD_1 | 196 | 198 | PF00675 | 0.796 |
CLV_NRD_NRD_1 | 200 | 202 | PF00675 | 0.672 |
CLV_NRD_NRD_1 | 33 | 35 | PF00675 | 0.822 |
CLV_NRD_NRD_1 | 447 | 449 | PF00675 | 0.461 |
CLV_NRD_NRD_1 | 99 | 101 | PF00675 | 0.732 |
CLV_PCSK_FUR_1 | 197 | 201 | PF00082 | 0.820 |
CLV_PCSK_FUR_1 | 445 | 449 | PF00082 | 0.417 |
CLV_PCSK_KEX2_1 | 115 | 117 | PF00082 | 0.793 |
CLV_PCSK_KEX2_1 | 196 | 198 | PF00082 | 0.791 |
CLV_PCSK_KEX2_1 | 199 | 201 | PF00082 | 0.687 |
CLV_PCSK_KEX2_1 | 33 | 35 | PF00082 | 0.822 |
CLV_PCSK_KEX2_1 | 447 | 449 | PF00082 | 0.437 |
CLV_PCSK_KEX2_1 | 99 | 101 | PF00082 | 0.688 |
CLV_PCSK_PC1ET2_1 | 99 | 101 | PF00082 | 0.590 |
CLV_PCSK_PC7_1 | 111 | 117 | PF00082 | 0.734 |
CLV_PCSK_PC7_1 | 196 | 202 | PF00082 | 0.702 |
CLV_PCSK_SKI1_1 | 201 | 205 | PF00082 | 0.699 |
CLV_PCSK_SKI1_1 | 283 | 287 | PF00082 | 0.459 |
CLV_PCSK_SKI1_1 | 298 | 302 | PF00082 | 0.303 |
CLV_PCSK_SKI1_1 | 457 | 461 | PF00082 | 0.719 |
DEG_APCC_DBOX_1 | 319 | 327 | PF00400 | 0.430 |
DEG_APCC_DBOX_1 | 446 | 454 | PF00400 | 0.424 |
DEG_SPOP_SBC_1 | 203 | 207 | PF00917 | 0.787 |
DEG_SPOP_SBC_1 | 28 | 32 | PF00917 | 0.599 |
DOC_CYCLIN_RxL_1 | 241 | 252 | PF00134 | 0.626 |
DOC_MAPK_gen_1 | 318 | 326 | PF00069 | 0.501 |
DOC_MAPK_JIP1_4 | 320 | 326 | PF00069 | 0.430 |
DOC_PP1_RVXF_1 | 418 | 424 | PF00149 | 0.382 |
DOC_PP4_FxxP_1 | 140 | 143 | PF00568 | 0.811 |
DOC_PP4_FxxP_1 | 335 | 338 | PF00568 | 0.376 |
DOC_USP7_MATH_1 | 224 | 228 | PF00917 | 0.737 |
DOC_USP7_MATH_1 | 27 | 31 | PF00917 | 0.727 |
DOC_USP7_MATH_1 | 46 | 50 | PF00917 | 0.518 |
DOC_USP7_MATH_1 | 77 | 81 | PF00917 | 0.836 |
DOC_USP7_MATH_1 | 94 | 98 | PF00917 | 0.470 |
DOC_WW_Pin1_4 | 217 | 222 | PF00397 | 0.736 |
DOC_WW_Pin1_4 | 410 | 415 | PF00397 | 0.501 |
LIG_14-3-3_CanoR_1 | 100 | 106 | PF00244 | 0.739 |
LIG_14-3-3_CanoR_1 | 312 | 317 | PF00244 | 0.551 |
LIG_14-3-3_CanoR_1 | 381 | 388 | PF00244 | 0.543 |
LIG_14-3-3_CanoR_1 | 45 | 51 | PF00244 | 0.831 |
LIG_BRCT_BRCA1_1 | 136 | 140 | PF00533 | 0.835 |
LIG_BRCT_BRCA1_1 | 292 | 296 | PF00533 | 0.501 |
LIG_deltaCOP1_diTrp_1 | 288 | 296 | PF00928 | 0.357 |
LIG_EH_1 | 332 | 336 | PF12763 | 0.430 |
LIG_FHA_1 | 127 | 133 | PF00498 | 0.744 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.738 |
LIG_FHA_1 | 311 | 317 | PF00498 | 0.630 |
LIG_FHA_1 | 435 | 441 | PF00498 | 0.440 |
LIG_FHA_1 | 458 | 464 | PF00498 | 0.681 |
LIG_FHA_2 | 176 | 182 | PF00498 | 0.739 |
LIG_LIR_Apic_2 | 137 | 143 | PF02991 | 0.821 |
LIG_LIR_Apic_2 | 348 | 354 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 104 | 108 | PF02991 | 0.515 |
LIG_LIR_Nem_3 | 398 | 402 | PF02991 | 0.344 |
LIG_MYND_1 | 334 | 338 | PF01753 | 0.430 |
LIG_SH2_NCK_1 | 257 | 261 | PF00017 | 0.430 |
LIG_SH2_STAP1 | 360 | 364 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 245 | 248 | PF00017 | 0.576 |
LIG_SH3_3 | 218 | 224 | PF00018 | 0.528 |
LIG_SH3_3 | 369 | 375 | PF00018 | 0.472 |
LIG_TRAF2_1 | 223 | 226 | PF00917 | 0.650 |
LIG_TRAF2_1 | 389 | 392 | PF00917 | 0.690 |
LIG_TRAF2_1 | 73 | 76 | PF00917 | 0.712 |
LIG_TRAF2_1 | 80 | 83 | PF00917 | 0.702 |
MOD_CK1_1 | 134 | 140 | PF00069 | 0.542 |
MOD_CK1_1 | 342 | 348 | PF00069 | 0.435 |
MOD_CK1_1 | 390 | 396 | PF00069 | 0.627 |
MOD_CK2_1 | 171 | 177 | PF00069 | 0.691 |
MOD_CK2_1 | 181 | 187 | PF00069 | 0.726 |
MOD_CK2_1 | 219 | 225 | PF00069 | 0.766 |
MOD_CK2_1 | 69 | 75 | PF00069 | 0.705 |
MOD_CK2_1 | 77 | 83 | PF00069 | 0.738 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.673 |
MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.541 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.641 |
MOD_GlcNHglycan | 166 | 169 | PF01048 | 0.700 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.719 |
MOD_GlcNHglycan | 275 | 278 | PF01048 | 0.417 |
MOD_GlcNHglycan | 292 | 295 | PF01048 | 0.283 |
MOD_GlcNHglycan | 340 | 344 | PF01048 | 0.320 |
MOD_GlcNHglycan | 383 | 386 | PF01048 | 0.561 |
MOD_GlcNHglycan | 40 | 43 | PF01048 | 0.762 |
MOD_GlcNHglycan | 96 | 99 | PF01048 | 0.770 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.839 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.752 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.767 |
MOD_GSK3_1 | 410 | 417 | PF00069 | 0.455 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.760 |
MOD_LATS_1 | 455 | 461 | PF00433 | 0.706 |
MOD_N-GLC_1 | 215 | 220 | PF02516 | 0.540 |
MOD_N-GLC_1 | 310 | 315 | PF02516 | 0.651 |
MOD_N-GLC_2 | 303 | 305 | PF02516 | 0.382 |
MOD_N-GLC_2 | 91 | 93 | PF02516 | 0.646 |
MOD_NEK2_1 | 117 | 122 | PF00069 | 0.595 |
MOD_NEK2_1 | 273 | 278 | PF00069 | 0.501 |
MOD_NEK2_1 | 379 | 384 | PF00069 | 0.499 |
MOD_NEK2_1 | 60 | 65 | PF00069 | 0.698 |
MOD_PIKK_1 | 181 | 187 | PF00454 | 0.824 |
MOD_PIKK_1 | 379 | 385 | PF00454 | 0.659 |
MOD_PKA_1 | 101 | 107 | PF00069 | 0.737 |
MOD_PKA_2 | 101 | 107 | PF00069 | 0.740 |
MOD_PKA_2 | 110 | 116 | PF00069 | 0.741 |
MOD_PKA_2 | 164 | 170 | PF00069 | 0.752 |
MOD_PKA_2 | 311 | 317 | PF00069 | 0.558 |
MOD_PKA_2 | 356 | 362 | PF00069 | 0.385 |
MOD_PKA_2 | 68 | 74 | PF00069 | 0.753 |
MOD_PKA_2 | 7 | 13 | PF00069 | 0.730 |
MOD_Plk_1 | 390 | 396 | PF00069 | 0.598 |
MOD_Plk_1 | 432 | 438 | PF00069 | 0.376 |
MOD_Plk_1 | 60 | 66 | PF00069 | 0.704 |
MOD_Plk_2-3 | 142 | 148 | PF00069 | 0.799 |
MOD_Plk_2-3 | 62 | 68 | PF00069 | 0.515 |
MOD_Plk_4 | 345 | 351 | PF00069 | 0.399 |
MOD_Plk_4 | 390 | 396 | PF00069 | 0.666 |
MOD_Plk_4 | 62 | 68 | PF00069 | 0.539 |
MOD_ProDKin_1 | 217 | 223 | PF00069 | 0.735 |
MOD_ProDKin_1 | 410 | 416 | PF00069 | 0.501 |
MOD_SUMO_for_1 | 16 | 19 | PF00179 | 0.639 |
MOD_SUMO_rev_2 | 19 | 28 | PF00179 | 0.699 |
MOD_SUMO_rev_2 | 340 | 348 | PF00179 | 0.376 |
MOD_SUMO_rev_2 | 410 | 419 | PF00179 | 0.410 |
TRG_DiLeu_BaEn_4 | 391 | 397 | PF01217 | 0.660 |
TRG_ENDOCYTIC_2 | 245 | 248 | PF00928 | 0.528 |
TRG_ER_diArg_1 | 108 | 111 | PF00400 | 0.719 |
TRG_ER_diArg_1 | 115 | 117 | PF00400 | 0.802 |
TRG_ER_diArg_1 | 196 | 199 | PF00400 | 0.791 |
TRG_ER_diArg_1 | 445 | 448 | PF00400 | 0.445 |
TRG_NLS_MonoCore_2 | 98 | 103 | PF00514 | 0.511 |
TRG_NLS_MonoExtN_4 | 99 | 104 | PF00514 | 0.687 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IKX8 | Leptomonas seymouri | 51% | 98% |
A0A0S4JTC6 | Bodo saltans | 37% | 100% |
A0A3Q8IEK2 | Leishmania donovani | 85% | 100% |
A4HHL8 | Leishmania braziliensis | 73% | 100% |
A4I4S7 | Leishmania infantum | 86% | 100% |
E9AE80 | Leishmania major | 86% | 100% |