GapMind for catabolism of small carbon sources

 

Alignments for a candidate for liuA in Derxia gummosa DSM 723

Align acyl-CoA dehydrogenase subunit (EC 1.3.8.4; EC 1.3.8.5) (characterized)
to candidate WP_028312267.1 H566_RS0116330 acyl-CoA dehydrogenase

Query= metacyc::MONOMER-11693
         (386 letters)



>NCBI__GCF_000482785.1:WP_028312267.1
          Length = 596

 Score = 99.8 bits (247), Expect = 2e-25
 Identities = 100/370 (27%), Positives = 161/370 (43%), Gaps = 57/370 (15%)

Query: 58  EYGGMGGDYLALGIALEELARVDSSVAITLEAGVSLGAMP-IHLFGTDAQKAEWLPRLCS 116
           ++GG G  Y+ L  A  E+    ++ A  +  G++ GA   +H  G++  KA +LP+L S
Sbjct: 101 DHGGQGLPYV-LNTAFFEMGN-SANQAWLMYPGLTHGAYECLHAHGSEELKAAYLPKLVS 158

Query: 117 GEILGAFGLTEPDGGSDAGATRTTARLDESTNEWVINGTKCFITNSGTDITGLVT--VTA 174
           GE LG   LTEP  G+D G  RT A        + I G+K FI+    D+T  +   V A
Sbjct: 159 GEWLGTMCLTEPHCGTDLGLLRTKA-TPRDDGSYAITGSKIFISAGEHDMTPNIVHLVLA 217

Query: 175 VTGRKPDGKPLISSIIVPSGTP----------GFTVAAPYSKVGWNASDTRELSFADVRV 224
                P+G   IS  +VP   P          G   A    K+G +A+ T +L   D R 
Sbjct: 218 RLPGAPEGSKGISLFLVPKFVPAADGSPGERNGLFCAGIEHKMGIHANATCQLVLEDAR- 276

Query: 225 PAANLLGEQGRGYAQFLRILDEGRIAISALATGLAQGCVDESVKYAGERHAFGRNI---- 280
               L+GE  RG A    +++  R+A+   + GL +     +  YA +R   GR +    
Sbjct: 277 --GWLIGEPHRGLAAMFVMMNAARVAVGVQSLGLGEVAYQNAAAYAKDRRQ-GRALTGPA 333

Query: 281 ---------------------------GAYQAIQFKIADMEMKAHMARVGWRDAASRLVA 313
                                      GA   + +    ++++ H       D  +R  A
Sbjct: 334 EPDKPADTLLVHPDVRRMLLTARAYTEGARALLYYTALQIDIEHHHP-----DEDARRDA 388

Query: 314 GEPFKKEAAIAKLYSSTVAVDNAREATQIHGGYGFMNEYPVARMWRDSKILEIGEGTSEV 373
            +       I K + +      A  A Q+ GG+G+++E+ V +  RD++I  I EGT+ V
Sbjct: 389 ADVVALLTPICKAFVTDNGFTAATAAQQVFGGHGYIHEWGVEQFVRDARINMIYEGTNGV 448

Query: 374 QRM-LIAREL 382
           Q + L+ R++
Sbjct: 449 QALDLLGRKV 458


Lambda     K      H
   0.318    0.136    0.402 

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: 642
Number of extensions: 45
Number of successful extensions: 3
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 386
Length of database: 596
Length adjustment: 34
Effective length of query: 352
Effective length of database: 562
Effective search space:   197824
Effective search space used:   197824
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: 51 (24.3 bits)

This GapMind analysis is from Sep 24 2021. 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