GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glucosaminate-lyase in Moritella dasanensis ArB 0140

Align Glucosaminate ammonia-lyase; EC 4.3.1.9; D-glucosaminate dehydratase alpha-subunit; GlcNA-DH alpha subunit; GlcNADH-alpha (uncharacterized)
to candidate WP_017223705.1 A923_RS0121265 thioredoxin-disulfide reductase

Query= curated2:Q93HX6
         (320 letters)



>NCBI__GCF_000276805.1:WP_017223705.1
          Length = 318

 Score =  459 bits (1180), Expect = e-134
 Identities = 227/316 (71%), Positives = 259/316 (81%), Gaps = 1/316 (0%)

Query: 1   MVEVRHSRVIILGSGPAGYSAAVYAARANLKPLLITGMQAGGQLTTTTEVDNWPGDVHGL 60
           M  ++H R++ILGSGPAGY+AAVYAARANL P+LITG+Q GGQLTTTTEV+NWPGD  GL
Sbjct: 1   MSNIKHCRLLILGSGPAGYTAAVYAARANLNPVLITGIQQGGQLTTTTEVENWPGDAEGL 60

Query: 61  TGPALMERMREHAERFETEIVFDHINAVDFAAKPYTLTGDSATYTCDALIIATGASARYL 120
           TGPALMERM+EHAERFETEIVFDHIN VD + +P+ L G+   YTCDALII TGASA+YL
Sbjct: 61  TGPALMERMKEHAERFETEIVFDHINDVDLSVRPFKLKGNDVEYTCDALIICTGASAKYL 120

Query: 121 GLPSEEAFMGKGVSACATCDGFFYRNKPVAVVGGGNTAVEEALYLANIASTVTLIHRRET 180
           GLPSEEAF G+GVSACATCDGFFYRN+ VAVVGGGNTAVEEALYL+NIAS V LIHRRE 
Sbjct: 121 GLPSEEAFKGRGVSACATCDGFFYRNQKVAVVGGGNTAVEEALYLSNIASEVHLIHRREE 180

Query: 181 FRAEKILIDKLNARVAEGKIILKLNANLDEVLGDNMGVTGARLKN-NDGSFDELKVDGVF 239
           FR+EKIL  +L  +VA G I L LN  LDEVLGD+MGVTG R+++       E  V G F
Sbjct: 181 FRSEKILTKRLQEKVANGNITLHLNKTLDEVLGDDMGVTGVRVRDTRTDEASEFDVMGAF 240

Query: 240 IAIGHTPNTSLFEGQLTLKDGYLVVQGGRDGNATATSVEGIFAAGDVADHVYRQAITSAG 299
           IAIGH PNT LF  QL +KDGYL V  G +G AT T++ G+FAAGDV+DH+YRQAITSAG
Sbjct: 241 IAIGHQPNTDLFIDQLDMKDGYLKVNSGTEGFATQTTIPGVFAAGDVSDHIYRQAITSAG 300

Query: 300 AGCMAALDTERYLDGL 315
            GCMAALD ER+LDGL
Sbjct: 301 TGCMAALDAERFLDGL 316


Lambda     K      H
   0.318    0.135    0.386 

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: 388
Number of extensions: 10
Number of successful extensions: 2
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: 320
Length of database: 318
Length adjustment: 28
Effective length of query: 292
Effective length of database: 290
Effective search space:    84680
Effective search space used:    84680
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: 48 (23.1 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