GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fucO in Sinorhizobium fredii NGR234

Align L-lactaldehyde reductase (EC 1.1.1.77) (characterized)
to candidate WP_012708668.1 NGR_RS21905 iron-containing alcohol dehydrogenase

Query= metacyc::STM4044-MONOMER
         (382 letters)



>NCBI__GCF_000018545.1:WP_012708668.1
          Length = 381

 Score =  206 bits (524), Expect = 9e-58
 Identities = 122/374 (32%), Positives = 193/374 (51%), Gaps = 13/374 (3%)

Query: 14  GAGAIADMVNLVANKQWGKALIVTDGQLVKLGLLDSLFSALDEHQMSYHLFDEVFPNPTE 73
           GAG I ++ +        K L++TD  L  + +       L+   +   +F +V PNP +
Sbjct: 16  GAGRIKELADHCKAVGMKKPLLITDRGLAPMAITQDALDILEGGGLGRAIFADVDPNPND 75

Query: 74  ELVQKGFAAYQSAECDYIIAFGGGSPIDTAKAVKILTANPGPSTAYSGVGKV-KNAGV-- 130
             ++ G  A++    D ++AFGGGS +D  K V  +     P   +  VG   K A V  
Sbjct: 76  RNLEAGIKAFKDGGHDGVVAFGGGSGLDLGKCVAFMVGQTRPVWDFEDVGDWWKRASVEG 135

Query: 131 --PLVAINTTAGTAAEMTSNAVIIDSARKVKEVIIDPNIIPDIAVDDASVMLEIPASVTA 188
             P++A+ TTAGT +E+   +VI +SA  VK+VI  P  +P + + D  + + +P  +TA
Sbjct: 136 IAPIIAVPTTAGTGSEVGRASVITNSASHVKKVIFHPKFLPAVTICDPELTVGMPKVITA 195

Query: 189 ATGMDALTHAVEAYVSVGAHPLTDANALEAIRLINLWLPKAVDDGHNLEAREQMAFGQYL 248
            TGMDA  H +EAY S   HP++   ALE +RL+  +LP+A  DG ++EAR  M     +
Sbjct: 196 GTGMDAFAHCLEAYSSPFYHPMSAGIALEGMRLVKEYLPRAYRDGADIEARANMMSAAAM 255

Query: 249 AGMAFNSAGLGLVHALAHQPGATHNLPHGVCNAILLPIVENFNRPNAVARFARIAQAMGV 308
             +AF   GLG +H+L+H  GA +N  HG+ NA+++P V  FNRP    + A  A  +G+
Sbjct: 256 GAVAFQK-GLGAIHSLSHPVGAIYNTHHGMTNAVVMPPVLRFNRPAIEEKIASAAAYLGI 314

Query: 309 ETRGMSDEAASQEAINAIRTLSKRVGIPEGFSKLGVTKEDIEGWLDKALADPCAPCNPRT 368
                          + +  L + +G+P   + LGV  + I+   + A+ DP A  NP  
Sbjct: 315 -------AGGFDGFYDYVLQLREELGVPNKLAALGVGTDRIDEMAEMAIVDPTASGNPVE 367

Query: 369 ASRDEVRGLYLEAL 382
            + D  R L+ E +
Sbjct: 368 LTLDAARKLFGECI 381


Lambda     K      H
   0.317    0.133    0.384 

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: 414
Number of extensions: 28
Number of successful extensions: 4
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: 382
Length of database: 381
Length adjustment: 30
Effective length of query: 352
Effective length of database: 351
Effective search space:   123552
Effective search space used:   123552
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: 50 (23.9 bits)

This GapMind analysis is from Apr 09 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