GapMind for catabolism of small carbon sources

 

Alignments for a candidate for etoh-dh-nad in Halomonas desiderata SP1

Align Alcohol dehydrogenase; EC 1.1.1.1; EC 1.1.1.4; EC 1.2.1.3 (characterized)
to candidate WP_086510909.1 BZY95_RS16090 NAD(P)-dependent alcohol dehydrogenase

Query= SwissProt::Q0KDL6
         (366 letters)



>NCBI__GCF_002151265.1:WP_086510909.1
          Length = 359

 Score =  573 bits (1478), Expect = e-168
 Identities = 280/364 (76%), Positives = 319/364 (87%), Gaps = 7/364 (1%)

Query: 1   MTAMMKAAVFVEPGRIELADKPIPDIGPNDALVRITTTTICGTDVHILKGEYPVAKGLTV 60
           M AMMKAA+FVEPGRIE+ DKPIPDIGPNDAL+R+TTTTICGTDVHILKGEYPVA+GLT+
Sbjct: 1   MPAMMKAAIFVEPGRIEIDDKPIPDIGPNDALIRVTTTTICGTDVHILKGEYPVARGLTI 60

Query: 61  GHEPVGIIEKLGSAVTGYREGQRVIAGAICPNFNSYAAQDGVASQDGSYLMASGQCGCHG 120
           GHEPVG+IEKLG+ V GY+EGQRVIAGAICP+F SYA QDG  +QDG +         HG
Sbjct: 61  GHEPVGVIEKLGANVRGYQEGQRVIAGAICPSFTSYACQDGCCAQDGGH-------HAHG 113

Query: 121 YKATAGWRFGNMIDGTQAEYVLVPDAQANLTPIPDGLTDEQVLMCPDIMSTGFKGAENAN 180
           YK   GWRFGN IDG QAEY+LVPDAQANL P+PDGLTDEQVLMCPDIMSTGF GAE+A 
Sbjct: 114 YKPMGGWRFGNTIDGAQAEYLLVPDAQANLAPVPDGLTDEQVLMCPDIMSTGFAGAESAG 173

Query: 181 IRIGDTVAVFAQGPIGLCATAGARLCGATTIIAIDGNDHRLEIARKMGADVVLNFRNCDV 240
           I+IGD+VAVFAQGPIGLCATAGARL GA  IIA+DG D RL +AR+MGADV L+FR  DV
Sbjct: 174 IKIGDSVAVFAQGPIGLCATAGARLRGAGLIIAVDGVDERLAMARQMGADVTLDFRKVDV 233

Query: 241 VDEVMKLTGGRGVDASIEALGTQATFEQSLRVLKPGGTLSSLGVYSSDLTIPLSAFAAGL 300
           V+E++++TGGRGVDASIEALG Q+TFE +LRV+KPGGTLSSLGVYSSDLTIPL AF AGL
Sbjct: 234 VEEILRITGGRGVDASIEALGLQSTFEAALRVVKPGGTLSSLGVYSSDLTIPLGAFCAGL 293

Query: 301 GDHKINTALCPGGKERMRRLINVIESGRVDLGALVTHQYRLDDIVAAYDLFANQRDGVLK 360
           GDHKI T+LCPGGKERMRRL+ VIE+GR+DLG +VTH+Y L DIV AYDLF++QRDGVLK
Sbjct: 294 GDHKIVTSLCPGGKERMRRLMQVIETGRIDLGPMVTHRYALADIVEAYDLFSHQRDGVLK 353

Query: 361 IAIK 364
           +AI+
Sbjct: 354 VAIQ 357


Lambda     K      H
   0.320    0.138    0.408 

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: 603
Number of extensions: 18
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: 366
Length of database: 359
Length adjustment: 29
Effective length of query: 337
Effective length of database: 330
Effective search space:   111210
Effective search space used:   111210
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 bits)
S2: 49 (23.5 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