GapMind for catabolism of small carbon sources

 

Alignments for a candidate for L-LDH in Caulobacter crescentus NA1000

Align L-lactate dehydrogenase (cytochrome) (EC 1.1.2.3) (characterized)
to candidate CCNA_01209 CCNA_01209 L-lactate dehydrogenase

Query= reanno::WCS417:GFF3737
         (376 letters)



>FitnessBrowser__Caulo:CCNA_01209
          Length = 383

 Score =  527 bits (1357), Expect = e-154
 Identities = 258/375 (68%), Positives = 305/375 (81%)

Query: 1   MIISSASDYRAAAKRKLPRFLFDYIDGGAYAEHTLRANSSDLAEISLRQRILRNVDNLSL 60
           MI+SS +D+R AA+R+LPRFLFDYIDGGAYAE T+  N  DLA+I+LRQR+L +V  +  
Sbjct: 1   MIVSSTTDFREAARRRLPRFLFDYIDGGAYAERTMARNIDDLADIALRQRVLMDVSVVDP 60

Query: 61  KTTLFGQELDMPVILSPVGLTGMYARRGEVQAAKAAANKGIPFCLSTVSVCPIEEVASQS 120
            TTLFG    +PV L+PVGLTGMYARRGE QAA+AAA KG+PFCLSTVSVC ++EV + S
Sbjct: 61  STTLFGVRQALPVALAPVGLTGMYARRGECQAARAAAAKGVPFCLSTVSVCDVDEVRAAS 120

Query: 121 AQAIWFQLYVLKDRGFMRNALERAQAAGVTTLVFTVDMPTPGARYRDAHSGMSGPFAAQR 180
           A   WFQLYVL+DRGFMR+ L RA AAG TTLVFTVDMP PGARYRDAHSGMSGP AA R
Sbjct: 121 ATPFWFQLYVLRDRGFMRDLLARASAAGATTLVFTVDMPVPGARYRDAHSGMSGPNAAAR 180

Query: 181 RMLQAVTKPQWAFDVGLMGRPHDLGNISKYLGKPTHLEDYIGWLANNFDASISWKDLEWI 240
           R++QA  KP WA+DVG+MG PH LGN++  LGK + L+D++GWLA NFD SI W DL+WI
Sbjct: 181 RLVQAALKPAWAWDVGVMGHPHRLGNVAPALGKASGLQDFMGWLAANFDPSIQWSDLKWI 240

Query: 241 REFWKGPMIIKGILDPQDAKDAVSFGADGIVVSNHGGRQLDGVLSTAKALPPIADAVGDD 300
           R+ WKGP++IKG+LDP+DAK A   GADG+VVSNHGGRQLDGVLS+A+ALP IADAVGD 
Sbjct: 241 RDAWKGPLVIKGVLDPEDAKAAADIGADGVVVSNHGGRQLDGVLSSARALPAIADAVGDR 300

Query: 301 LTVLVDSGIRSGLDVVRMLALGAKACLLGRATAYALAADGQHGVENLLDIFAKEMRVAMT 360
           LTVL D G+RSGLDVVRMLALGA+  L+GRA AYALAA G+ GV  LLD+  KEMRVAM 
Sbjct: 301 LTVLADGGVRSGLDVVRMLALGARGVLIGRAYAYALAARGEAGVTQLLDLIDKEMRVAMA 360

Query: 361 LTGVTSIAQIDRSTL 375
           LTGV  +A I+ + L
Sbjct: 361 LTGVRDVASINETIL 375


Lambda     K      H
   0.321    0.136    0.401 

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: 467
Number of extensions: 12
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: 376
Length of database: 383
Length adjustment: 30
Effective length of query: 346
Effective length of database: 353
Effective search space:   122138
Effective search space used:   122138
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