Metal Binding, Uncharacterized
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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 4 |
GO:0004784 | superoxide dismutase activity | 2 | 4 |
GO:0005488 | binding | 1 | 4 |
GO:0016209 | antioxidant activity | 1 | 4 |
GO:0016491 | oxidoreductase activity | 2 | 4 |
GO:0016721 | oxidoreductase activity, acting on superoxide radicals as acceptor | 3 | 4 |
GO:0043167 | ion binding | 2 | 4 |
GO:0043169 | cation binding | 3 | 4 |
GO:0046872 | metal ion binding | 4 | 4 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 216 | 220 | PF00656 | 0.568 |
CLV_C14_Caspase3-7 | 465 | 469 | PF00656 | 0.413 |
CLV_C14_Caspase3-7 | 474 | 478 | PF00656 | 0.427 |
CLV_NRD_NRD_1 | 11 | 13 | PF00675 | 0.482 |
CLV_NRD_NRD_1 | 22 | 24 | PF00675 | 0.633 |
CLV_NRD_NRD_1 | 292 | 294 | PF00675 | 0.476 |
CLV_NRD_NRD_1 | 300 | 302 | PF00675 | 0.618 |
CLV_PCSK_KEX2_1 | 11 | 13 | PF00082 | 0.408 |
CLV_PCSK_KEX2_1 | 201 | 203 | PF00082 | 0.376 |
CLV_PCSK_KEX2_1 | 22 | 24 | PF00082 | 0.498 |
CLV_PCSK_PC1ET2_1 | 201 | 203 | PF00082 | 0.376 |
CLV_PCSK_SKI1_1 | 11 | 15 | PF00082 | 0.428 |
CLV_PCSK_SKI1_1 | 46 | 50 | PF00082 | 0.652 |
DEG_APCC_DBOX_1 | 10 | 18 | PF00400 | 0.488 |
DEG_APCC_DBOX_1 | 75 | 83 | PF00400 | 0.456 |
DEG_SCF_FBW7_1 | 160 | 167 | PF00400 | 0.393 |
DEG_SPOP_SBC_1 | 352 | 356 | PF00917 | 0.619 |
DOC_CKS1_1 | 161 | 166 | PF01111 | 0.384 |
DOC_CYCLIN_RxL_1 | 57 | 65 | PF00134 | 0.388 |
DOC_CYCLIN_RxL_1 | 9 | 20 | PF00134 | 0.496 |
DOC_MAPK_DCC_7 | 11 | 19 | PF00069 | 0.450 |
DOC_MAPK_FxFP_2 | 455 | 458 | PF00069 | 0.529 |
DOC_MAPK_gen_1 | 11 | 19 | PF00069 | 0.405 |
DOC_MAPK_gen_1 | 60 | 66 | PF00069 | 0.561 |
DOC_MAPK_MEF2A_6 | 11 | 19 | PF00069 | 0.465 |
DOC_PP2B_LxvP_1 | 177 | 180 | PF13499 | 0.463 |
DOC_PP4_FxxP_1 | 455 | 458 | PF00568 | 0.529 |
DOC_USP7_MATH_1 | 146 | 150 | PF00917 | 0.331 |
DOC_USP7_MATH_1 | 208 | 212 | PF00917 | 0.507 |
DOC_USP7_MATH_1 | 27 | 31 | PF00917 | 0.433 |
DOC_USP7_MATH_1 | 352 | 356 | PF00917 | 0.762 |
DOC_USP7_MATH_1 | 377 | 381 | PF00917 | 0.795 |
DOC_USP7_MATH_1 | 389 | 393 | PF00917 | 0.598 |
DOC_USP7_MATH_1 | 44 | 48 | PF00917 | 0.558 |
DOC_WW_Pin1_4 | 151 | 156 | PF00397 | 0.511 |
DOC_WW_Pin1_4 | 160 | 165 | PF00397 | 0.475 |
DOC_WW_Pin1_4 | 229 | 234 | PF00397 | 0.568 |
DOC_WW_Pin1_4 | 337 | 342 | PF00397 | 0.658 |
LIG_14-3-3_CanoR_1 | 231 | 237 | PF00244 | 0.555 |
LIG_14-3-3_CanoR_1 | 256 | 264 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 471 | 476 | PF00244 | 0.402 |
LIG_14-3-3_CanoR_1 | 76 | 86 | PF00244 | 0.323 |
LIG_Actin_WH2_2 | 303 | 319 | PF00022 | 0.572 |
LIG_BRCT_BRCA1_1 | 333 | 337 | PF00533 | 0.614 |
LIG_BRCT_BRCA1_1 | 90 | 94 | PF00533 | 0.300 |
LIG_deltaCOP1_diTrp_1 | 441 | 448 | PF00928 | 0.331 |
LIG_EH1_1 | 28 | 36 | PF00400 | 0.508 |
LIG_FHA_1 | 118 | 124 | PF00498 | 0.432 |
LIG_FHA_1 | 161 | 167 | PF00498 | 0.443 |
LIG_FHA_1 | 26 | 32 | PF00498 | 0.597 |
LIG_FHA_1 | 280 | 286 | PF00498 | 0.364 |
LIG_FHA_1 | 324 | 330 | PF00498 | 0.522 |
LIG_FHA_1 | 371 | 377 | PF00498 | 0.695 |
LIG_FHA_1 | 442 | 448 | PF00498 | 0.457 |
LIG_FHA_1 | 459 | 465 | PF00498 | 0.399 |
LIG_FHA_2 | 239 | 245 | PF00498 | 0.679 |
LIG_FHA_2 | 294 | 300 | PF00498 | 0.484 |
LIG_FHA_2 | 451 | 457 | PF00498 | 0.432 |
LIG_FHA_2 | 472 | 478 | PF00498 | 0.403 |
LIG_LIR_Apic_2 | 452 | 458 | PF02991 | 0.400 |
LIG_LIR_LC3C_4 | 33 | 36 | PF02991 | 0.294 |
LIG_LIR_Nem_3 | 132 | 138 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 326 | 331 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 91 | 97 | PF02991 | 0.454 |
LIG_Pex14_1 | 418 | 422 | PF04695 | 0.391 |
LIG_Pex14_2 | 94 | 98 | PF04695 | 0.437 |
LIG_SH2_CRK | 135 | 139 | PF00017 | 0.420 |
LIG_SH2_CRK | 162 | 166 | PF00017 | 0.483 |
LIG_SH2_SRC | 475 | 478 | PF00017 | 0.561 |
LIG_SH2_STAP1 | 288 | 292 | PF00017 | 0.445 |
LIG_SH2_STAP1 | 40 | 44 | PF00017 | 0.502 |
LIG_SH2_STAT5 | 162 | 165 | PF00017 | 0.378 |
LIG_SH2_STAT5 | 88 | 91 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 97 | 100 | PF00017 | 0.472 |
LIG_SH3_3 | 158 | 164 | PF00018 | 0.494 |
LIG_SH3_3 | 335 | 341 | PF00018 | 0.602 |
LIG_SH3_3 | 373 | 379 | PF00018 | 0.642 |
LIG_Sin3_3 | 32 | 39 | PF02671 | 0.297 |
LIG_TRAF2_1 | 241 | 244 | PF00917 | 0.572 |
LIG_WRC_WIRS_1 | 16 | 21 | PF05994 | 0.488 |
MOD_CDC14_SPxK_1 | 154 | 157 | PF00782 | 0.482 |
MOD_CDK_SPK_2 | 229 | 234 | PF00069 | 0.515 |
MOD_CDK_SPxK_1 | 151 | 157 | PF00069 | 0.503 |
MOD_CK1_1 | 134 | 140 | PF00069 | 0.473 |
MOD_CK1_1 | 259 | 265 | PF00069 | 0.467 |
MOD_CK1_1 | 30 | 36 | PF00069 | 0.485 |
MOD_CK1_1 | 333 | 339 | PF00069 | 0.621 |
MOD_CK1_1 | 340 | 346 | PF00069 | 0.589 |
MOD_CK1_1 | 355 | 361 | PF00069 | 0.497 |
MOD_CK1_1 | 442 | 448 | PF00069 | 0.498 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.375 |
MOD_CK2_1 | 164 | 170 | PF00069 | 0.621 |
MOD_CK2_1 | 238 | 244 | PF00069 | 0.697 |
MOD_CK2_1 | 293 | 299 | PF00069 | 0.488 |
MOD_CK2_1 | 450 | 456 | PF00069 | 0.402 |
MOD_CK2_1 | 476 | 482 | PF00069 | 0.434 |
MOD_Cter_Amidation | 20 | 23 | PF01082 | 0.584 |
MOD_GlcNHglycan | 166 | 169 | PF01048 | 0.643 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.527 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.559 |
MOD_GlcNHglycan | 269 | 272 | PF01048 | 0.516 |
MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.438 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.509 |
MOD_GlcNHglycan | 347 | 350 | PF01048 | 0.730 |
MOD_GlcNHglycan | 357 | 360 | PF01048 | 0.486 |
MOD_GlcNHglycan | 362 | 366 | PF01048 | 0.518 |
MOD_GlcNHglycan | 379 | 382 | PF01048 | 0.724 |
MOD_GlcNHglycan | 391 | 394 | PF01048 | 0.688 |
MOD_GlcNHglycan | 40 | 43 | PF01048 | 0.591 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.476 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.312 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.679 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.565 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.337 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.496 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.568 |
MOD_GSK3_1 | 351 | 358 | PF00069 | 0.465 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.718 |
MOD_GSK3_1 | 385 | 392 | PF00069 | 0.697 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.468 |
MOD_GSK3_1 | 437 | 444 | PF00069 | 0.518 |
MOD_N-GLC_1 | 196 | 201 | PF02516 | 0.356 |
MOD_N-GLC_1 | 345 | 350 | PF02516 | 0.560 |
MOD_N-GLC_1 | 423 | 428 | PF02516 | 0.417 |
MOD_N-GLC_1 | 458 | 463 | PF02516 | 0.415 |
MOD_N-GLC_1 | 49 | 54 | PF02516 | 0.550 |
MOD_NEK2_1 | 141 | 146 | PF00069 | 0.466 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.466 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.681 |
MOD_NEK2_1 | 279 | 284 | PF00069 | 0.475 |
MOD_NEK2_1 | 316 | 321 | PF00069 | 0.501 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.491 |
MOD_NEK2_2 | 443 | 448 | PF00069 | 0.314 |
MOD_PIKK_1 | 293 | 299 | PF00454 | 0.398 |
MOD_PIKK_1 | 311 | 317 | PF00454 | 0.558 |
MOD_PIKK_1 | 368 | 374 | PF00454 | 0.725 |
MOD_PK_1 | 248 | 254 | PF00069 | 0.525 |
MOD_PK_1 | 256 | 262 | PF00069 | 0.370 |
MOD_PKA_1 | 293 | 299 | PF00069 | 0.370 |
MOD_PKA_2 | 21 | 27 | PF00069 | 0.609 |
MOD_PKA_2 | 255 | 261 | PF00069 | 0.376 |
MOD_PKA_2 | 470 | 476 | PF00069 | 0.361 |
MOD_Plk_1 | 131 | 137 | PF00069 | 0.498 |
MOD_Plk_1 | 361 | 367 | PF00069 | 0.708 |
MOD_Plk_1 | 381 | 387 | PF00069 | 0.505 |
MOD_Plk_1 | 458 | 464 | PF00069 | 0.412 |
MOD_Plk_1 | 69 | 75 | PF00069 | 0.449 |
MOD_Plk_4 | 172 | 178 | PF00069 | 0.352 |
MOD_Plk_4 | 30 | 36 | PF00069 | 0.489 |
MOD_Plk_4 | 333 | 339 | PF00069 | 0.654 |
MOD_Plk_4 | 443 | 449 | PF00069 | 0.487 |
MOD_Plk_4 | 450 | 456 | PF00069 | 0.363 |
MOD_Plk_4 | 459 | 465 | PF00069 | 0.340 |
MOD_Plk_4 | 62 | 68 | PF00069 | 0.368 |
MOD_ProDKin_1 | 151 | 157 | PF00069 | 0.503 |
MOD_ProDKin_1 | 160 | 166 | PF00069 | 0.487 |
MOD_ProDKin_1 | 229 | 235 | PF00069 | 0.575 |
MOD_ProDKin_1 | 337 | 343 | PF00069 | 0.657 |
MOD_SUMO_for_1 | 359 | 362 | PF00179 | 0.613 |
MOD_SUMO_rev_2 | 93 | 103 | PF00179 | 0.463 |
TRG_DiLeu_BaEn_1 | 9 | 14 | PF01217 | 0.349 |
TRG_DiLeu_BaLyEn_6 | 12 | 17 | PF01217 | 0.374 |
TRG_DiLeu_LyEn_5 | 9 | 14 | PF01217 | 0.462 |
TRG_ENDOCYTIC_2 | 135 | 138 | PF00928 | 0.412 |
TRG_ER_diArg_1 | 10 | 12 | PF00400 | 0.391 |
TRG_Pf-PMV_PEXEL_1 | 201 | 205 | PF00026 | 0.421 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P312 | Leptomonas seymouri | 49% | 95% |
A0A1X0PA30 | Trypanosomatidae | 36% | 100% |
A0A3Q8IHA9 | Leishmania donovani | 100% | 100% |
A0A3R7K8T3 | Trypanosoma rangeli | 37% | 100% |
A4HAI1 | Leishmania braziliensis | 80% | 100% |
C9ZN11 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
E9B4P2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q4Q3D4 | Leishmania major | 92% | 100% |
V5DAY1 | Trypanosoma cruzi | 36% | 100% |