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: A4I6M3
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 3 |
GO:0003677 | DNA binding | 4 | 3 |
GO:0005488 | binding | 1 | 3 |
GO:0097159 | organic cyclic compound binding | 2 | 3 |
GO:1901363 | heterocyclic compound binding | 2 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 254 | 258 | PF00656 | 0.514 |
CLV_C14_Caspase3-7 | 411 | 415 | PF00656 | 0.734 |
CLV_NRD_NRD_1 | 164 | 166 | PF00675 | 0.651 |
CLV_NRD_NRD_1 | 196 | 198 | PF00675 | 0.709 |
CLV_NRD_NRD_1 | 278 | 280 | PF00675 | 0.668 |
CLV_NRD_NRD_1 | 333 | 335 | PF00675 | 0.737 |
CLV_NRD_NRD_1 | 360 | 362 | PF00675 | 0.639 |
CLV_NRD_NRD_1 | 378 | 380 | PF00675 | 0.781 |
CLV_NRD_NRD_1 | 382 | 384 | PF00675 | 0.699 |
CLV_PCSK_FUR_1 | 276 | 280 | PF00082 | 0.664 |
CLV_PCSK_FUR_1 | 331 | 335 | PF00082 | 0.824 |
CLV_PCSK_FUR_1 | 357 | 361 | PF00082 | 0.741 |
CLV_PCSK_KEX2_1 | 162 | 164 | PF00082 | 0.675 |
CLV_PCSK_KEX2_1 | 192 | 194 | PF00082 | 0.699 |
CLV_PCSK_KEX2_1 | 196 | 198 | PF00082 | 0.704 |
CLV_PCSK_KEX2_1 | 211 | 213 | PF00082 | 0.687 |
CLV_PCSK_KEX2_1 | 278 | 280 | PF00082 | 0.658 |
CLV_PCSK_KEX2_1 | 282 | 284 | PF00082 | 0.644 |
CLV_PCSK_KEX2_1 | 331 | 333 | PF00082 | 0.753 |
CLV_PCSK_KEX2_1 | 356 | 358 | PF00082 | 0.730 |
CLV_PCSK_KEX2_1 | 359 | 361 | PF00082 | 0.701 |
CLV_PCSK_KEX2_1 | 378 | 380 | PF00082 | 0.590 |
CLV_PCSK_PC1ET2_1 | 162 | 164 | PF00082 | 0.719 |
CLV_PCSK_PC1ET2_1 | 192 | 194 | PF00082 | 0.699 |
CLV_PCSK_PC1ET2_1 | 211 | 213 | PF00082 | 0.687 |
CLV_PCSK_PC1ET2_1 | 282 | 284 | PF00082 | 0.716 |
CLV_PCSK_PC1ET2_1 | 356 | 358 | PF00082 | 0.730 |
CLV_PCSK_PC7_1 | 158 | 164 | PF00082 | 0.748 |
CLV_PCSK_PC7_1 | 274 | 280 | PF00082 | 0.818 |
CLV_PCSK_SKI1_1 | 115 | 119 | PF00082 | 0.588 |
CLV_PCSK_SKI1_1 | 223 | 227 | PF00082 | 0.780 |
CLV_PCSK_SKI1_1 | 283 | 287 | PF00082 | 0.711 |
CLV_PCSK_SKI1_1 | 336 | 340 | PF00082 | 0.751 |
CLV_PCSK_SKI1_1 | 84 | 88 | PF00082 | 0.637 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.640 |
DEG_SPOP_SBC_1 | 183 | 187 | PF00917 | 0.683 |
DEG_SPOP_SBC_1 | 93 | 97 | PF00917 | 0.654 |
DOC_CYCLIN_RxL_1 | 111 | 120 | PF00134 | 0.587 |
DOC_MAPK_gen_1 | 192 | 203 | PF00069 | 0.724 |
DOC_MAPK_gen_1 | 381 | 391 | PF00069 | 0.690 |
DOC_MAPK_gen_1 | 91 | 100 | PF00069 | 0.556 |
DOC_USP7_MATH_1 | 174 | 178 | PF00917 | 0.585 |
DOC_USP7_MATH_1 | 206 | 210 | PF00917 | 0.748 |
DOC_USP7_MATH_1 | 248 | 252 | PF00917 | 0.569 |
DOC_USP7_MATH_1 | 398 | 402 | PF00917 | 0.745 |
DOC_USP7_MATH_1 | 407 | 411 | PF00917 | 0.738 |
DOC_USP7_MATH_1 | 82 | 86 | PF00917 | 0.522 |
DOC_USP7_MATH_1 | 93 | 97 | PF00917 | 0.621 |
DOC_USP7_UBL2_3 | 162 | 166 | PF12436 | 0.730 |
DOC_USP7_UBL2_3 | 188 | 192 | PF12436 | 0.761 |
DOC_USP7_UBL2_3 | 207 | 211 | PF12436 | 0.537 |
DOC_WW_Pin1_4 | 133 | 138 | PF00397 | 0.680 |
DOC_WW_Pin1_4 | 156 | 161 | PF00397 | 0.759 |
DOC_WW_Pin1_4 | 21 | 26 | PF00397 | 0.541 |
DOC_WW_Pin1_4 | 308 | 313 | PF00397 | 0.777 |
LIG_14-3-3_CanoR_1 | 12 | 19 | PF00244 | 0.542 |
LIG_14-3-3_CanoR_1 | 199 | 204 | PF00244 | 0.720 |
LIG_14-3-3_CanoR_1 | 223 | 232 | PF00244 | 0.645 |
LIG_14-3-3_CanoR_1 | 276 | 286 | PF00244 | 0.781 |
LIG_14-3-3_CanoR_1 | 44 | 53 | PF00244 | 0.491 |
LIG_14-3-3_CanoR_1 | 70 | 77 | PF00244 | 0.524 |
LIG_14-3-3_CanoR_1 | 94 | 99 | PF00244 | 0.570 |
LIG_Actin_WH2_2 | 69 | 86 | PF00022 | 0.588 |
LIG_BRCT_BRCA1_1 | 363 | 367 | PF00533 | 0.707 |
LIG_BRCT_BRCA1_1 | 47 | 51 | PF00533 | 0.632 |
LIG_CAP-Gly_1 | 414 | 419 | PF01302 | 0.729 |
LIG_FHA_1 | 170 | 176 | PF00498 | 0.718 |
LIG_FHA_1 | 37 | 43 | PF00498 | 0.508 |
LIG_FHA_1 | 93 | 99 | PF00498 | 0.588 |
LIG_FHA_2 | 143 | 149 | PF00498 | 0.768 |
LIG_FHA_2 | 224 | 230 | PF00498 | 0.816 |
LIG_FHA_2 | 279 | 285 | PF00498 | 0.684 |
LIG_FHA_2 | 297 | 303 | PF00498 | 0.708 |
LIG_FHA_2 | 309 | 315 | PF00498 | 0.613 |
LIG_FHA_2 | 345 | 351 | PF00498 | 0.704 |
LIG_LIR_Gen_1 | 54 | 64 | PF02991 | 0.572 |
LIG_LIR_Nem_3 | 301 | 307 | PF02991 | 0.572 |
LIG_LIR_Nem_3 | 54 | 60 | PF02991 | 0.623 |
LIG_PDZ_Class_2 | 414 | 419 | PF00595 | 0.807 |
LIG_Rb_pABgroove_1 | 112 | 120 | PF01858 | 0.547 |
LIG_SH2_NCK_1 | 307 | 311 | PF00017 | 0.587 |
LIG_SH2_SRC | 307 | 310 | PF00017 | 0.586 |
LIG_SH2_STAP1 | 9 | 13 | PF00017 | 0.476 |
LIG_SH3_1 | 266 | 272 | PF00018 | 0.721 |
LIG_SH3_2 | 269 | 274 | PF14604 | 0.814 |
LIG_SH3_3 | 134 | 140 | PF00018 | 0.697 |
LIG_SH3_3 | 164 | 170 | PF00018 | 0.734 |
LIG_SH3_3 | 188 | 194 | PF00018 | 0.592 |
LIG_SH3_3 | 266 | 272 | PF00018 | 0.799 |
LIG_SH3_4 | 405 | 412 | PF00018 | 0.700 |
MOD_CDK_SPK_2 | 156 | 161 | PF00069 | 0.653 |
MOD_CDK_SPxK_1 | 156 | 162 | PF00069 | 0.654 |
MOD_CDK_SPxxK_3 | 156 | 163 | PF00069 | 0.654 |
MOD_CK1_1 | 21 | 27 | PF00069 | 0.771 |
MOD_CK1_1 | 227 | 233 | PF00069 | 0.753 |
MOD_CK1_1 | 34 | 40 | PF00069 | 0.498 |
MOD_CK2_1 | 14 | 20 | PF00069 | 0.531 |
MOD_CK2_1 | 142 | 148 | PF00069 | 0.809 |
MOD_CK2_1 | 223 | 229 | PF00069 | 0.655 |
MOD_CK2_1 | 278 | 284 | PF00069 | 0.690 |
MOD_CK2_1 | 308 | 314 | PF00069 | 0.688 |
MOD_CK2_1 | 344 | 350 | PF00069 | 0.747 |
MOD_CK2_1 | 398 | 404 | PF00069 | 0.718 |
MOD_Cter_Amidation | 163 | 166 | PF01082 | 0.692 |
MOD_Cter_Amidation | 194 | 197 | PF01082 | 0.685 |
MOD_Cter_Amidation | 276 | 279 | PF01082 | 0.782 |
MOD_Cter_Amidation | 357 | 360 | PF01082 | 0.703 |
MOD_Cter_Amidation | 376 | 379 | PF01082 | 0.606 |
MOD_GlcNHglycan | 119 | 122 | PF01048 | 0.606 |
MOD_GlcNHglycan | 130 | 133 | PF01048 | 0.510 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.556 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.799 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.743 |
MOD_GlcNHglycan | 238 | 241 | PF01048 | 0.672 |
MOD_GlcNHglycan | 248 | 251 | PF01048 | 0.591 |
MOD_GlcNHglycan | 375 | 378 | PF01048 | 0.652 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.578 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.523 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.514 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.801 |
MOD_GSK3_1 | 223 | 230 | PF00069 | 0.650 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.747 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.646 |
MOD_NEK2_1 | 117 | 122 | PF00069 | 0.564 |
MOD_NEK2_1 | 18 | 23 | PF00069 | 0.568 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.650 |
MOD_NEK2_1 | 213 | 218 | PF00069 | 0.683 |
MOD_NEK2_1 | 392 | 397 | PF00069 | 0.820 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.585 |
MOD_NEK2_2 | 260 | 265 | PF00069 | 0.585 |
MOD_NEK2_2 | 36 | 41 | PF00069 | 0.606 |
MOD_PIKK_1 | 392 | 398 | PF00454 | 0.820 |
MOD_PK_1 | 94 | 100 | PF00069 | 0.568 |
MOD_PKA_1 | 278 | 284 | PF00069 | 0.674 |
MOD_PKA_1 | 373 | 379 | PF00069 | 0.689 |
MOD_PKA_2 | 107 | 113 | PF00069 | 0.556 |
MOD_PKA_2 | 213 | 219 | PF00069 | 0.721 |
MOD_PKA_2 | 277 | 283 | PF00069 | 0.684 |
MOD_PKA_2 | 291 | 297 | PF00069 | 0.565 |
MOD_PKA_2 | 93 | 99 | PF00069 | 0.637 |
MOD_PKB_1 | 197 | 205 | PF00069 | 0.719 |
MOD_PKB_1 | 276 | 284 | PF00069 | 0.709 |
MOD_PKB_1 | 359 | 367 | PF00069 | 0.726 |
MOD_Plk_1 | 234 | 240 | PF00069 | 0.684 |
MOD_Plk_2-3 | 344 | 350 | PF00069 | 0.747 |
MOD_Plk_4 | 14 | 20 | PF00069 | 0.531 |
MOD_Plk_4 | 82 | 88 | PF00069 | 0.521 |
MOD_ProDKin_1 | 133 | 139 | PF00069 | 0.684 |
MOD_ProDKin_1 | 156 | 162 | PF00069 | 0.760 |
MOD_ProDKin_1 | 21 | 27 | PF00069 | 0.549 |
MOD_ProDKin_1 | 308 | 314 | PF00069 | 0.782 |
TRG_ER_diArg_1 | 196 | 199 | PF00400 | 0.710 |
TRG_ER_diArg_1 | 212 | 215 | PF00400 | 0.746 |
TRG_ER_diArg_1 | 273 | 276 | PF00400 | 0.678 |
TRG_ER_diArg_1 | 331 | 334 | PF00400 | 0.752 |
TRG_ER_diArg_1 | 357 | 360 | PF00400 | 0.740 |
TRG_ER_diArg_1 | 378 | 381 | PF00400 | 0.821 |
TRG_NLS_Bipartite_1 | 192 | 214 | PF00514 | 0.793 |
TRG_NLS_MonoCore_2 | 164 | 169 | PF00514 | 0.680 |
TRG_NLS_MonoCore_2 | 203 | 208 | PF00514 | 0.569 |
TRG_NLS_MonoExtC_3 | 160 | 165 | PF00514 | 0.704 |
TRG_NLS_MonoExtC_3 | 209 | 214 | PF00514 | 0.765 |
TRG_NLS_MonoExtC_3 | 355 | 360 | PF00514 | 0.701 |
TRG_NLS_MonoExtN_4 | 158 | 165 | PF00514 | 0.706 |
TRG_NLS_MonoExtN_4 | 207 | 214 | PF00514 | 0.769 |
TRG_Pf-PMV_PEXEL_1 | 115 | 119 | PF00026 | 0.609 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IIK0 | Leptomonas seymouri | 35% | 100% |
A0A3S7X4A5 | Leishmania donovani | 99% | 100% |
A4HJ79 | Leishmania braziliensis | 59% | 100% |
E9B1P6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
Q4Q6G4 | Leishmania major | 84% | 97% |