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 | 0.736 |
CLV_C14_Caspase3-7 | 464 | 468 | PF00656 | 0.454 |
CLV_C14_Caspase3-7 | 473 | 477 | PF00656 | 0.470 |
CLV_NRD_NRD_1 | 11 | 13 | PF00675 | 0.527 |
CLV_NRD_NRD_1 | 22 | 24 | PF00675 | 0.667 |
CLV_NRD_NRD_1 | 232 | 234 | PF00675 | 0.518 |
CLV_NRD_NRD_1 | 300 | 302 | PF00675 | 0.605 |
CLV_PCSK_KEX2_1 | 11 | 13 | PF00082 | 0.577 |
CLV_PCSK_KEX2_1 | 201 | 203 | PF00082 | 0.485 |
CLV_PCSK_KEX2_1 | 22 | 24 | PF00082 | 0.568 |
CLV_PCSK_PC1ET2_1 | 201 | 203 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 11 | 15 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 125 | 129 | PF00082 | 0.439 |
CLV_PCSK_SKI1_1 | 46 | 50 | PF00082 | 0.642 |
CLV_PCSK_SKI1_1 | 470 | 474 | PF00082 | 0.346 |
DEG_APCC_DBOX_1 | 10 | 18 | PF00400 | 0.529 |
DEG_APCC_DBOX_1 | 232 | 240 | PF00400 | 0.668 |
DEG_APCC_DBOX_1 | 75 | 83 | PF00400 | 0.504 |
DEG_SCF_FBW7_1 | 160 | 167 | PF00400 | 0.497 |
DEG_SPOP_SBC_1 | 352 | 356 | PF00917 | 0.764 |
DOC_CKS1_1 | 161 | 166 | PF01111 | 0.487 |
DOC_CYCLIN_RxL_1 | 122 | 132 | PF00134 | 0.439 |
DOC_CYCLIN_RxL_1 | 9 | 18 | PF00134 | 0.490 |
DOC_MAPK_DCC_7 | 11 | 19 | PF00069 | 0.582 |
DOC_MAPK_FxFP_2 | 454 | 457 | PF00069 | 0.568 |
DOC_MAPK_gen_1 | 11 | 19 | PF00069 | 0.505 |
DOC_MAPK_gen_1 | 60 | 66 | PF00069 | 0.581 |
DOC_MAPK_MEF2A_6 | 11 | 19 | PF00069 | 0.514 |
DOC_PP2B_LxvP_1 | 177 | 180 | PF13499 | 0.507 |
DOC_PP2B_LxvP_1 | 62 | 65 | PF13499 | 0.327 |
DOC_PP4_FxxP_1 | 454 | 457 | PF00568 | 0.568 |
DOC_USP7_MATH_1 | 208 | 212 | PF00917 | 0.570 |
DOC_USP7_MATH_1 | 27 | 31 | PF00917 | 0.547 |
DOC_USP7_MATH_1 | 325 | 329 | PF00917 | 0.656 |
DOC_USP7_MATH_1 | 352 | 356 | PF00917 | 0.741 |
DOC_USP7_MATH_1 | 360 | 364 | PF00917 | 0.719 |
DOC_USP7_MATH_1 | 376 | 380 | PF00917 | 0.804 |
DOC_USP7_MATH_1 | 388 | 392 | PF00917 | 0.654 |
DOC_USP7_MATH_1 | 44 | 48 | PF00917 | 0.603 |
DOC_WW_Pin1_4 | 151 | 156 | PF00397 | 0.557 |
DOC_WW_Pin1_4 | 160 | 165 | PF00397 | 0.514 |
LIG_14-3-3_CanoR_1 | 109 | 118 | PF00244 | 0.538 |
LIG_14-3-3_CanoR_1 | 231 | 237 | PF00244 | 0.632 |
LIG_14-3-3_CanoR_1 | 470 | 475 | PF00244 | 0.442 |
LIG_Actin_WH2_2 | 303 | 319 | PF00022 | 0.621 |
LIG_AP2alpha_1 | 94 | 98 | PF02296 | 0.327 |
LIG_BRCT_BRCA1_1 | 333 | 337 | PF00533 | 0.751 |
LIG_BRCT_BRCA1_1 | 90 | 94 | PF00533 | 0.364 |
LIG_EH1_1 | 28 | 36 | PF00400 | 0.542 |
LIG_FHA_1 | 118 | 124 | PF00498 | 0.568 |
LIG_FHA_1 | 161 | 167 | PF00498 | 0.459 |
LIG_FHA_1 | 26 | 32 | PF00498 | 0.616 |
LIG_FHA_1 | 280 | 286 | PF00498 | 0.476 |
LIG_FHA_1 | 324 | 330 | PF00498 | 0.609 |
LIG_FHA_1 | 370 | 376 | PF00498 | 0.735 |
LIG_FHA_1 | 425 | 431 | PF00498 | 0.512 |
LIG_FHA_1 | 437 | 443 | PF00498 | 0.518 |
LIG_FHA_1 | 458 | 464 | PF00498 | 0.427 |
LIG_FHA_2 | 239 | 245 | PF00498 | 0.722 |
LIG_FHA_2 | 294 | 300 | PF00498 | 0.540 |
LIG_FHA_2 | 450 | 456 | PF00498 | 0.458 |
LIG_FHA_2 | 471 | 477 | PF00498 | 0.456 |
LIG_LIR_Apic_2 | 451 | 457 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 132 | 138 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 91 | 97 | PF02991 | 0.492 |
LIG_Pex14_1 | 417 | 421 | PF04695 | 0.458 |
LIG_Pex14_2 | 94 | 98 | PF04695 | 0.450 |
LIG_SH2_CRK | 135 | 139 | PF00017 | 0.527 |
LIG_SH2_CRK | 162 | 166 | PF00017 | 0.527 |
LIG_SH2_SRC | 474 | 477 | PF00017 | 0.593 |
LIG_SH2_STAP1 | 40 | 44 | PF00017 | 0.590 |
LIG_SH2_STAT5 | 162 | 165 | PF00017 | 0.552 |
LIG_SH2_STAT5 | 88 | 91 | PF00017 | 0.478 |
LIG_SH2_STAT5 | 97 | 100 | PF00017 | 0.511 |
LIG_SH3_3 | 158 | 164 | PF00018 | 0.491 |
LIG_SH3_3 | 372 | 378 | PF00018 | 0.792 |
LIG_TRAF2_1 | 241 | 244 | PF00917 | 0.663 |
LIG_UBA3_1 | 176 | 183 | PF00899 | 0.396 |
LIG_WRC_WIRS_1 | 16 | 21 | PF05994 | 0.555 |
MOD_CDC14_SPxK_1 | 154 | 157 | PF00782 | 0.526 |
MOD_CDK_SPxK_1 | 151 | 157 | PF00069 | 0.547 |
MOD_CK1_1 | 134 | 140 | PF00069 | 0.556 |
MOD_CK1_1 | 259 | 265 | PF00069 | 0.459 |
MOD_CK1_1 | 30 | 36 | PF00069 | 0.475 |
MOD_CK1_1 | 333 | 339 | PF00069 | 0.678 |
MOD_CK1_1 | 340 | 346 | PF00069 | 0.655 |
MOD_CK1_1 | 441 | 447 | PF00069 | 0.505 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.473 |
MOD_CK2_1 | 164 | 170 | PF00069 | 0.586 |
MOD_CK2_1 | 238 | 244 | PF00069 | 0.745 |
MOD_CK2_1 | 286 | 292 | PF00069 | 0.510 |
MOD_CK2_1 | 293 | 299 | PF00069 | 0.514 |
MOD_CK2_1 | 338 | 344 | PF00069 | 0.625 |
MOD_CK2_1 | 449 | 455 | PF00069 | 0.462 |
MOD_CK2_1 | 475 | 481 | PF00069 | 0.486 |
MOD_Cter_Amidation | 20 | 23 | PF01082 | 0.716 |
MOD_GlcNHglycan | 166 | 169 | PF01048 | 0.657 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.556 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.501 |
MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.480 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.545 |
MOD_GlcNHglycan | 340 | 343 | PF01048 | 0.698 |
MOD_GlcNHglycan | 347 | 350 | PF01048 | 0.711 |
MOD_GlcNHglycan | 356 | 359 | PF01048 | 0.697 |
MOD_GlcNHglycan | 361 | 365 | PF01048 | 0.758 |
MOD_GlcNHglycan | 378 | 381 | PF01048 | 0.765 |
MOD_GlcNHglycan | 390 | 393 | PF01048 | 0.746 |
MOD_GlcNHglycan | 40 | 43 | PF01048 | 0.577 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.573 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.522 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.636 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.529 |
MOD_GSK3_1 | 276 | 283 | PF00069 | 0.417 |
MOD_GSK3_1 | 287 | 294 | PF00069 | 0.407 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.341 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.577 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.631 |
MOD_GSK3_1 | 376 | 383 | PF00069 | 0.751 |
MOD_GSK3_1 | 384 | 391 | PF00069 | 0.742 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.504 |
MOD_GSK3_1 | 436 | 443 | PF00069 | 0.514 |
MOD_N-GLC_1 | 196 | 201 | PF02516 | 0.408 |
MOD_N-GLC_1 | 345 | 350 | PF02516 | 0.719 |
MOD_N-GLC_1 | 422 | 427 | PF02516 | 0.602 |
MOD_N-GLC_1 | 457 | 462 | PF02516 | 0.472 |
MOD_N-GLC_1 | 49 | 54 | PF02516 | 0.582 |
MOD_NEK2_1 | 141 | 146 | PF00069 | 0.503 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.479 |
MOD_NEK2_1 | 276 | 281 | PF00069 | 0.461 |
MOD_NEK2_1 | 316 | 321 | PF00069 | 0.535 |
MOD_NEK2_1 | 337 | 342 | PF00069 | 0.734 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.482 |
MOD_NEK2_1 | 442 | 447 | PF00069 | 0.388 |
MOD_PIKK_1 | 276 | 282 | PF00454 | 0.380 |
MOD_PIKK_1 | 291 | 297 | PF00454 | 0.628 |
MOD_PIKK_1 | 311 | 317 | PF00454 | 0.334 |
MOD_PIKK_1 | 367 | 373 | PF00454 | 0.768 |
MOD_PK_1 | 256 | 262 | PF00069 | 0.456 |
MOD_PKA_2 | 21 | 27 | PF00069 | 0.647 |
MOD_PKA_2 | 232 | 238 | PF00069 | 0.604 |
MOD_Plk_1 | 131 | 137 | PF00069 | 0.519 |
MOD_Plk_1 | 360 | 366 | PF00069 | 0.747 |
MOD_Plk_1 | 457 | 463 | PF00069 | 0.468 |
MOD_Plk_1 | 69 | 75 | PF00069 | 0.489 |
MOD_Plk_4 | 141 | 147 | PF00069 | 0.534 |
MOD_Plk_4 | 30 | 36 | PF00069 | 0.527 |
MOD_Plk_4 | 333 | 339 | PF00069 | 0.699 |
MOD_Plk_4 | 442 | 448 | PF00069 | 0.452 |
MOD_Plk_4 | 449 | 455 | PF00069 | 0.419 |
MOD_Plk_4 | 458 | 464 | PF00069 | 0.385 |
MOD_ProDKin_1 | 151 | 157 | PF00069 | 0.547 |
MOD_ProDKin_1 | 160 | 166 | PF00069 | 0.525 |
MOD_SUMO_for_1 | 358 | 361 | PF00179 | 0.746 |
MOD_SUMO_rev_2 | 93 | 103 | PF00179 | 0.501 |
TRG_DiLeu_BaEn_1 | 9 | 14 | PF01217 | 0.408 |
TRG_DiLeu_BaLyEn_6 | 12 | 17 | PF01217 | 0.418 |
TRG_DiLeu_BaLyEn_6 | 172 | 177 | PF01217 | 0.457 |
TRG_DiLeu_BaLyEn_6 | 62 | 67 | PF01217 | 0.321 |
TRG_DiLeu_LyEn_5 | 9 | 14 | PF01217 | 0.506 |
TRG_ENDOCYTIC_2 | 135 | 138 | PF00928 | 0.523 |
TRG_ER_diArg_1 | 10 | 12 | PF00400 | 0.497 |
TRG_Pf-PMV_PEXEL_1 | 125 | 129 | PF00026 | 0.486 |
TRG_Pf-PMV_PEXEL_1 | 201 | 205 | PF00026 | 0.489 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P312 | Leptomonas seymouri | 48% | 95% |
A0A1X0PA30 | Trypanosomatidae | 36% | 100% |
A0A3Q8IHA9 | Leishmania donovani | 92% | 100% |
A0A3R7K8T3 | Trypanosoma rangeli | 36% | 100% |
A4HAI1 | Leishmania braziliensis | 81% | 100% |
A4IAP2 | Leishmania infantum | 92% | 100% |
C9ZN11 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
E9B4P2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
V5DAY1 | Trypanosoma cruzi | 36% | 100% |