GapMind for catabolism of small carbon sources

 

Alignments for a candidate for sdaB in Cereibacter sphaeroides ATCC 17029

Align Threonine dehydratase 2 biosynthetic, chloroplastic; SlTD2; Threonine deaminase 2; EC 4.3.1.17; EC 4.3.1.19 (characterized)
to candidate WP_009563248.1 RSPH17029_RS14480 threonine ammonia-lyase IlvA

Query= SwissProt::P25306
         (595 letters)



>NCBI__GCF_000015985.1:WP_009563248.1
          Length = 415

 Score =  193 bits (491), Expect = 1e-53
 Identities = 127/400 (31%), Positives = 204/400 (51%), Gaps = 9/400 (2%)

Query: 108 DVAIESPLELAEKLSDRLGVNFYIKREDKQRVFSFKLRGAYNMMSNLSREELD-KGVITA 166
           D+  E+PL+  + LS R G + ++KRED   V S+KLRGA+  M  +     D +  + A
Sbjct: 17  DLFPETPLQRNDHLSARYGADIWLKREDLTPVRSYKLRGAFTAMRKVRDARPDQRSFVCA 76

Query: 167 SAGNHAQGVALAGQRLNCVAKIVMPTTTPQIKIDAVRALGGD---VVLYGKTFDEAQTHA 223
           SAGNHAQGVA A +       I MP TTPQ KI   R  GG+   +VL G  FD+    A
Sbjct: 77  SAGNHAQGVAYACRHFGVKGTIFMPVTTPQQKIAKTRTFGGEAVEIVLTGDYFDQTLAAA 136

Query: 224 LELSEKDGLKYIPPFDDPGVIKGQGTIGTEINRQL-KDIHAVFIPVGGGGLIAGVATFFK 282
                +    ++ PFDDP VI+GQ ++G E+  QL +    V +PVGGGGL +GV  F +
Sbjct: 137 QAWCAEQKAHFLAPFDDPDVIEGQASVGVELLEQLGRAPDLVVLPVGGGGLASGVTAFLR 196

Query: 283 QIAPNTKIIGVEPYGAASMTLSLHEGHRVKLSNVDTFADGVAVALVGEYTFAKCQEL-ID 341
             AP T    VEP G AS+  +L  G    L  V++F DG AVA +G+  F+    +  D
Sbjct: 197 SEAPETDFRFVEPAGGASLLAALEAGGPTALPRVNSFVDGAAVARLGQLPFSMLDWVRPD 256

Query: 342 GMVLVANDGISAAIKDVYDEGRNILETSGAVAIAGAAAYCEFYKIKNENIVAIASGANMD 401
            + L   D I   + ++ +    +LE +GA+++       +  +I+   +V + SG N D
Sbjct: 257 QVHLAPEDRICITMLEMLNVEGIVLEPAGALSVDVLPELAD--RIRGRTVVCVTSGGNFD 314

Query: 402 FSKLHKVTELAGLGSGKEALLATFMVEQQGSFKTFVGLVG-SLNFTELTYRFTSERKNAL 460
           F +L +V E A   SG +      M ++ G+ + F+ ++G   +     Y   S R    
Sbjct: 315 FERLPEVKERAQRYSGLKKYFILRMPQRPGALREFLMMLGPDDDIARFEYLKKSARNFGS 374

Query: 461 ILYRVNVDKESDLEKMIEDMKSSNMTTLNLSHNELVVDHL 500
           +L  +   +  +  ++   M+ + +   +++ ++ + + L
Sbjct: 375 VLIGIETREAGNFARLTAVMEEAGLNYRDITGDDALAEFL 414


Lambda     K      H
   0.317    0.135    0.382 

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: 502
Number of extensions: 29
Number of successful extensions: 5
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 1
Number of HSP's successfully gapped: 1
Length of query: 595
Length of database: 415
Length adjustment: 34
Effective length of query: 561
Effective length of database: 381
Effective search space:   213741
Effective search space used:   213741
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 (21.7 bits)
S2: 52 (24.6 bits)

This GapMind analysis is from Apr 10 2024. The underlying query database was built on Sep 17 2021.

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About GapMind

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:

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

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