Align L-aspartate semialdehyde sulfurtransferase (EC 2.8.1.16) (characterized)
to candidate WP_011973508.1 MAEO_RS03970 CBS domain-containing protein
Query= BRENDA::Q57564 (509 letters) >NCBI__GCF_000017185.1:WP_011973508.1 Length = 511 Score = 726 bits (1875), Expect = 0.0 Identities = 351/506 (69%), Positives = 430/506 (84%), Gaps = 2/506 (0%) Query: 3 MKTIKEINEKIKKGEAVVVTAEEMIKIVEEEGAKRAADYVDVVTTGTFGAMCSSGVFINF 62 MKTI EINEKIK +AVVV AEEMIKIVE+ G+K A+ VD+VTTGTFGAMCSSG+F+NF Sbjct: 1 MKTIAEINEKIKNNDAVVVNAEEMIKIVEDIGSKNASKEVDIVTTGTFGAMCSSGIFLNF 60 Query: 63 GHSDPPIKMLRIYLNNVEAYGGLAAVDAYIGAAQPNEDPDVDIDYGGAHVIEDLVRGKEV 122 GHSDPPIKM++ YLN VEAY G+AAVDAY+GA QPN D D+DI+YGGAHVIEDLV KE+ Sbjct: 61 GHSDPPIKMIKTYLNGVEAYSGVAAVDAYLGATQPNSDDDIDINYGGAHVIEDLVAKKEI 120 Query: 123 ELYAEGYTTDCYPRKEVNVRITLDDVNQAIMVNPRNCYQTYAAATNSREEKIYTYMGILL 182 L AEGYTTDCYPRK+V+ IT+DD+NQAIM+NPRNCYQ+Y AATNS +EK+YTYMG LL Sbjct: 121 TLKAEGYTTDCYPRKKVSTTITIDDLNQAIMINPRNCYQSYVAATNSLDEKLYTYMGTLL 180 Query: 183 PEYNNVHYSGAGQLNPLQNDYNPETKSFNTIGIGTRIFLGGGIGYVIGEGTQHNP--PFG 240 PE N++YSGAGQLNPLQNDYN TKS+NTIGIGT+IFLGG GY+IGEGTQH+P FG Sbjct: 181 PELGNINYSGAGQLNPLQNDYNNTTKSYNTIGIGTKIFLGGAEGYIIGEGTQHSPDTKFG 240 Query: 241 TLMVKGDLKQMNPKFIRAATMPRYGSTLYVGIGIPIPVLNEKIAERCAIRDEDIEVPIYD 300 T+M+KGDLK+M+ K+IRA+T+P+YG +L+VG+G+PIPVLNE++A+ CAIRDEDIE+PI D Sbjct: 241 TIMIKGDLKEMDKKYIRASTIPKYGPSLFVGMGVPIPVLNEEVAKSCAIRDEDIEIPILD 300 Query: 301 YGFPRRDRPLIAKTNYKVLRSGKITLNVNIDGKDVEKTVKTGSVSSYKMAREVAETLKQW 360 YG RRDRP+I KTNYK LR+G+IT +NIDG+ +E+T+KT SVSSYK +RE+AE LK+W Sbjct: 301 YGVQRRDRPVIGKTNYKELRTGEITTKLNIDGEIIEETIKTASVSSYKKSREIAEELKKW 360 Query: 361 ILDGKFLLTERVDTLGRAENKPMKSPITLVKDILSKPPITAHSNISIMEAAKILIKHNIN 420 IL G FLLTERV+ L A KPMK+ LV DI+SKPPI A+ NISI EA+KILI++ IN Sbjct: 361 ILKGDFLLTERVNPLSYAAPKPMKAQAKLVGDIISKPPILANQNISINEASKILIENGIN 420 Query: 421 HLPIVDEHGKLVGIITSWDIAKALAQNKKTIEEIMTRNVITAHEDEPVDHVAIKMSKYNI 480 HLPIVDE+ LVGIITSWDIA+A+AQNK +I EIMT VI++ DEP+D +A KMS YNI Sbjct: 421 HLPIVDENKNLVGIITSWDIARAVAQNKNSILEIMTATVISSTVDEPIDVLARKMSIYNI 480 Query: 481 SGVPVVDDYRRVVGIVTSEDISRLFG 506 SG P++D ++VVG++T+ED+S+L G Sbjct: 481 SGAPILDKNKKVVGMITAEDLSKLVG 506 Lambda K H 0.317 0.137 0.393 Gapped Lambda K H 0.267 0.0410 0.140 Matrix: BLOSUM62 Gap Penalties: Existence: 11, Extension: 1 Number of Sequences: 1 Number of Hits to DB: 868 Number of extensions: 42 Number of successful extensions: 4 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 3 Number of HSP's successfully gapped: 3 Length of query: 509 Length of database: 511 Length adjustment: 34 Effective length of query: 475 Effective length of database: 477 Effective search space: 226575 Effective search space used: 226575 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.3 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.6 bits) S2: 52 (24.6 bits)
This GapMind analysis is from Apr 10 2024. The underlying query database was built on Apr 09 2024.
Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.
A candidate for a step is "high confidence" if either:
Otherwise, a candidate is "medium confidence" if either:
Other blast hits with at least 50% coverage are "low confidence."
Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:
GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).
For more information, see:
If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know
by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory