GapMind for catabolism of small carbon sources

 

Alignments for a candidate for L-LDH in Phaeobacter inhibens BS107

Align L-lactate dehydrogenase (cytochrome) (EC 1.1.2.3) (characterized)
to candidate GFF481 PGA1_c04920 l-lactate dehydrogenase IldD

Query= reanno::Smeli:SM_b20850
         (378 letters)



>FitnessBrowser__Phaeo:GFF481
          Length = 388

 Score =  511 bits (1316), Expect = e-149
 Identities = 253/373 (67%), Positives = 301/373 (80%)

Query: 1   MTQILEIRDLKALARRRVPKLFFDYADSGAWTEGTYRANEEDFAGIKLRQRVLVDMSDRS 60
           M  I  I DLK +  RRVP++F+DYA+SG+WTE T+R N  DF  I+LRQRV VDM+ RS
Sbjct: 1   MPVITNINDLKRIYERRVPRMFYDYAESGSWTEQTFRDNTNDFEKIRLRQRVAVDMAGRS 60

Query: 61  LETTMIGQKVSMPVALAPTGLTGMQHADGEMLAAQAAEAFGVPFTLSTMSICSIEDVASV 120
             + MIGQ VSMPVALAP GLTGMQHADGE+ AA+AAE FGVPFTLSTMSI SIE+VA  
Sbjct: 61  TASQMIGQDVSMPVALAPVGLTGMQHADGEIKAARAAETFGVPFTLSTMSINSIEEVAEA 120

Query: 121 TTKPFWFQLYVMREREFVLDLIDRAKAAKCSALVMTLDLQILGQRHKDLRNGLSAPPRLT 180
           TTKPFWFQLY M++ ++V  LI RAK A+CSALV+TLDLQILGQRHKDL+NGLSAPP+LT
Sbjct: 121 TTKPFWFQLYTMKDDDYVRRLIQRAKDARCSALVITLDLQILGQRHKDLKNGLSAPPKLT 180

Query: 181 PKHLWMMATRPGWCMKMLGTNRRTFRNIVGHAKSVADLSSLQAWTNEQFDPQLSWKDVEW 240
           PK +  + T+  W ++ML   RR F NIVGH + ++D SSL AWT EQFDP L W  +  
Sbjct: 181 PKTIANLMTKWSWGLQMLSAKRRNFGNIVGHVEGISDASSLGAWTAEQFDPSLDWSKIAK 240

Query: 241 IKERWGGPLILKGILDPEDAKMAAKTGADAIIVSNHGGRQLDGAHSSISMLPRIVEAVGD 300
           + E W G +ILKGILD EDAKMAAK GADAI+VSNHGGRQLDGA SSI MLP I++AVGD
Sbjct: 241 LIELWDGKVILKGILDVEDAKMAAKLGADAIVVSNHGGRQLDGALSSIQMLPAIMDAVGD 300

Query: 301 QIEVHLDGGIRSGQDVLKAIALGAKGTYIGRPFLYGLGALGKEGVTLALDIIRKEMDTTM 360
           QIEVHLD GIRSGQDVLKA+ALGAKGT IGR F+YGLGA+G+ GVT AL+++ KE+DTTM
Sbjct: 301 QIEVHLDSGIRSGQDVLKALALGAKGTMIGRAFVYGLGAMGQHGVTRALEVLHKELDTTM 360

Query: 361 ALCGKRRITEVGR 373
           ALCG++ + ++GR
Sbjct: 361 ALCGEKSVADLGR 373


Lambda     K      H
   0.321    0.136    0.406 

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: 494
Number of extensions: 18
Number of successful extensions: 1
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: 378
Length of database: 388
Length adjustment: 30
Effective length of query: 348
Effective length of database: 358
Effective search space:   124584
Effective search space used:   124584
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 (21.9 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Sep 17 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