Metal Binding, Zinc finger, C3HC4 type (RING finger), putative
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) | yes | yes: 3 |
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: A4HTV7
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 8 |
GO:0003677 | DNA binding | 4 | 8 |
GO:0005488 | binding | 1 | 8 |
GO:0097159 | organic cyclic compound binding | 2 | 8 |
GO:1901363 | heterocyclic compound binding | 2 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 226 | 230 | PF00656 | 0.730 |
CLV_C14_Caspase3-7 | 333 | 337 | PF00656 | 0.635 |
CLV_NRD_NRD_1 | 201 | 203 | PF00675 | 0.718 |
CLV_NRD_NRD_1 | 233 | 235 | PF00675 | 0.702 |
CLV_NRD_NRD_1 | 366 | 368 | PF00675 | 0.532 |
CLV_PCSK_FUR_1 | 199 | 203 | PF00082 | 0.726 |
CLV_PCSK_KEX2_1 | 14 | 16 | PF00082 | 0.455 |
CLV_PCSK_KEX2_1 | 201 | 203 | PF00082 | 0.722 |
CLV_PCSK_KEX2_1 | 233 | 235 | PF00082 | 0.702 |
CLV_PCSK_KEX2_1 | 366 | 368 | PF00082 | 0.564 |
CLV_PCSK_PC1ET2_1 | 14 | 16 | PF00082 | 0.455 |
CLV_PCSK_SKI1_1 | 136 | 140 | PF00082 | 0.565 |
CLV_PCSK_SKI1_1 | 319 | 323 | PF00082 | 0.831 |
CLV_PCSK_SKI1_1 | 350 | 354 | PF00082 | 0.739 |
CLV_PCSK_SKI1_1 | 42 | 46 | PF00082 | 0.401 |
DEG_APCC_DBOX_1 | 114 | 122 | PF00400 | 0.429 |
DEG_COP1_1 | 124 | 132 | PF00400 | 0.569 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.608 |
DEG_SPOP_SBC_1 | 342 | 346 | PF00917 | 0.752 |
DOC_CYCLIN_RxL_1 | 39 | 49 | PF00134 | 0.401 |
DOC_CYCLIN_yCln2_LP_2 | 213 | 216 | PF00134 | 0.744 |
DOC_CYCLIN_yCln2_LP_2 | 87 | 93 | PF00134 | 0.526 |
DOC_MAPK_MEF2A_6 | 122 | 129 | PF00069 | 0.590 |
DOC_PP2B_LxvP_1 | 127 | 130 | PF13499 | 0.573 |
DOC_PP2B_LxvP_1 | 213 | 216 | PF13499 | 0.744 |
DOC_PP2B_LxvP_1 | 443 | 446 | PF13499 | 0.401 |
DOC_PP2B_LxvP_1 | 45 | 48 | PF13499 | 0.455 |
DOC_PP2B_LxvP_1 | 85 | 88 | PF13499 | 0.401 |
DOC_PP4_FxxP_1 | 322 | 325 | PF00568 | 0.612 |
DOC_USP7_MATH_1 | 158 | 162 | PF00917 | 0.844 |
DOC_USP7_MATH_1 | 16 | 20 | PF00917 | 0.480 |
DOC_USP7_MATH_1 | 206 | 210 | PF00917 | 0.672 |
DOC_USP7_MATH_1 | 251 | 255 | PF00917 | 0.726 |
DOC_USP7_MATH_1 | 257 | 261 | PF00917 | 0.613 |
DOC_USP7_MATH_1 | 301 | 305 | PF00917 | 0.729 |
DOC_USP7_MATH_1 | 309 | 313 | PF00917 | 0.680 |
DOC_USP7_MATH_1 | 332 | 336 | PF00917 | 0.812 |
DOC_USP7_MATH_1 | 343 | 347 | PF00917 | 0.652 |
LIG_14-3-3_CanoR_1 | 20 | 27 | PF00244 | 0.455 |
LIG_14-3-3_CanoR_1 | 201 | 206 | PF00244 | 0.688 |
LIG_14-3-3_CanoR_1 | 233 | 240 | PF00244 | 0.694 |
LIG_14-3-3_CanoR_1 | 350 | 355 | PF00244 | 0.732 |
LIG_14-3-3_CanoR_1 | 58 | 68 | PF00244 | 0.526 |
LIG_BIR_III_4 | 386 | 390 | PF00653 | 0.574 |
LIG_BRCT_BRCA1_1 | 6 | 10 | PF00533 | 0.541 |
LIG_FHA_1 | 124 | 130 | PF00498 | 0.569 |
LIG_FHA_1 | 137 | 143 | PF00498 | 0.643 |
LIG_FHA_1 | 209 | 215 | PF00498 | 0.742 |
LIG_FHA_1 | 427 | 433 | PF00498 | 0.427 |
LIG_FHA_1 | 448 | 454 | PF00498 | 0.435 |
LIG_FHA_1 | 76 | 82 | PF00498 | 0.442 |
LIG_FHA_2 | 47 | 53 | PF00498 | 0.512 |
LIG_FHA_2 | 61 | 67 | PF00498 | 0.322 |
LIG_Integrin_isoDGR_2 | 165 | 167 | PF01839 | 0.710 |
LIG_LIR_Apic_2 | 320 | 325 | PF02991 | 0.613 |
LIG_LIR_Gen_1 | 116 | 125 | PF02991 | 0.521 |
LIG_LIR_Gen_1 | 79 | 90 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 66 | 71 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 79 | 85 | PF02991 | 0.401 |
LIG_PDZ_Class_3 | 462 | 467 | PF00595 | 0.606 |
LIG_SH2_NCK_1 | 306 | 310 | PF00017 | 0.826 |
LIG_SH2_STAT5 | 306 | 309 | PF00017 | 0.787 |
LIG_SH2_STAT5 | 405 | 408 | PF00017 | 0.539 |
LIG_SH2_STAT5 | 54 | 57 | PF00017 | 0.401 |
LIG_SH2_STAT5 | 82 | 85 | PF00017 | 0.401 |
LIG_SH3_3 | 174 | 180 | PF00018 | 0.702 |
LIG_SH3_3 | 378 | 384 | PF00018 | 0.513 |
LIG_SH3_3 | 443 | 449 | PF00018 | 0.498 |
LIG_SUMO_SIM_anti_2 | 429 | 434 | PF11976 | 0.455 |
LIG_TRAF2_1 | 312 | 315 | PF00917 | 0.691 |
LIG_WRC_WIRS_1 | 302 | 307 | PF05994 | 0.600 |
MOD_CK1_1 | 105 | 111 | PF00069 | 0.455 |
MOD_CK1_1 | 154 | 160 | PF00069 | 0.709 |
MOD_CK1_1 | 161 | 167 | PF00069 | 0.735 |
MOD_CK1_1 | 19 | 25 | PF00069 | 0.480 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.747 |
MOD_CK1_1 | 253 | 259 | PF00069 | 0.775 |
MOD_CK1_1 | 304 | 310 | PF00069 | 0.696 |
MOD_CK1_1 | 346 | 352 | PF00069 | 0.730 |
MOD_CK1_1 | 447 | 453 | PF00069 | 0.405 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.455 |
MOD_CK2_1 | 105 | 111 | PF00069 | 0.412 |
MOD_CK2_1 | 293 | 299 | PF00069 | 0.836 |
MOD_CK2_1 | 309 | 315 | PF00069 | 0.734 |
MOD_CK2_1 | 356 | 362 | PF00069 | 0.611 |
MOD_CK2_1 | 46 | 52 | PF00069 | 0.512 |
MOD_CK2_1 | 60 | 66 | PF00069 | 0.357 |
MOD_GlcNHglycan | 156 | 159 | PF01048 | 0.768 |
MOD_GlcNHglycan | 172 | 176 | PF01048 | 0.653 |
MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.698 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.788 |
MOD_GlcNHglycan | 235 | 238 | PF01048 | 0.672 |
MOD_GlcNHglycan | 243 | 247 | PF01048 | 0.642 |
MOD_GlcNHglycan | 252 | 256 | PF01048 | 0.713 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.420 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.401 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.704 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.693 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.723 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.693 |
MOD_GSK3_1 | 289 | 296 | PF00069 | 0.799 |
MOD_GSK3_1 | 342 | 349 | PF00069 | 0.657 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.415 |
MOD_N-GLC_1 | 105 | 110 | PF02516 | 0.427 |
MOD_N-GLC_1 | 158 | 163 | PF02516 | 0.782 |
MOD_N-GLC_1 | 30 | 35 | PF02516 | 0.449 |
MOD_NEK2_1 | 205 | 210 | PF00069 | 0.745 |
MOD_NEK2_1 | 232 | 237 | PF00069 | 0.787 |
MOD_NEK2_1 | 341 | 346 | PF00069 | 0.812 |
MOD_NEK2_2 | 301 | 306 | PF00069 | 0.695 |
MOD_OFUCOSY | 441 | 448 | PF10250 | 0.465 |
MOD_PIKK_1 | 206 | 212 | PF00454 | 0.758 |
MOD_PIKK_1 | 309 | 315 | PF00454 | 0.711 |
MOD_PKA_1 | 201 | 207 | PF00069 | 0.716 |
MOD_PKA_1 | 233 | 239 | PF00069 | 0.695 |
MOD_PKA_2 | 19 | 25 | PF00069 | 0.455 |
MOD_PKA_2 | 201 | 207 | PF00069 | 0.686 |
MOD_PKA_2 | 232 | 238 | PF00069 | 0.807 |
MOD_PKB_1 | 149 | 157 | PF00069 | 0.720 |
MOD_PKB_1 | 199 | 207 | PF00069 | 0.707 |
MOD_Plk_1 | 105 | 111 | PF00069 | 0.412 |
MOD_Plk_1 | 30 | 36 | PF00069 | 0.449 |
MOD_Plk_1 | 4 | 10 | PF00069 | 0.556 |
MOD_Plk_4 | 208 | 214 | PF00069 | 0.743 |
MOD_Plk_4 | 272 | 278 | PF00069 | 0.758 |
MOD_Plk_4 | 301 | 307 | PF00069 | 0.735 |
MOD_Plk_4 | 343 | 349 | PF00069 | 0.813 |
MOD_Plk_4 | 426 | 432 | PF00069 | 0.366 |
TRG_DiLeu_BaLyEn_6 | 393 | 398 | PF01217 | 0.572 |
TRG_ENDOCYTIC_2 | 68 | 71 | PF00928 | 0.366 |
TRG_ENDOCYTIC_2 | 82 | 85 | PF00928 | 0.401 |
TRG_ER_diArg_1 | 199 | 202 | PF00400 | 0.710 |
TRG_ER_diArg_1 | 232 | 234 | PF00400 | 0.700 |
TRG_ER_diArg_1 | 366 | 369 | PF00400 | 0.618 |
TRG_ER_diArg_1 | 394 | 397 | PF00400 | 0.569 |
TRG_ER_FFAT_2 | 299 | 310 | PF00635 | 0.603 |
TRG_Pf-PMV_PEXEL_1 | 366 | 370 | PF00026 | 0.559 |
TRG_Pf-PMV_PEXEL_1 | 396 | 401 | PF00026 | 0.560 |
TRG_Pf-PMV_PEXEL_1 | 42 | 46 | PF00026 | 0.401 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I698 | Leptomonas seymouri | 62% | 97% |
A0A3S5H6D0 | Leishmania donovani | 100% | 100% |
A4H5L9 | Leishmania braziliensis | 75% | 98% |
E9AMP4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q4QHY1 | Leishmania major | 96% | 100% |
V5BIH0 | Trypanosoma cruzi | 38% | 100% |