GapMind for catabolism of small carbon sources

 

Alignments for a candidate for proW in Thiomicrorhabdus arctica DSM 13458

Align Glycine betaine/proline betaine transport system permease protein ProW (characterized)
to candidate WP_019557546.1 F612_RS0109560 proline/glycine betaine ABC transporter permease ProW

Query= SwissProt::P14176
         (354 letters)



>NCBI__GCF_000381085.1:WP_019557546.1
          Length = 359

 Score =  401 bits (1031), Expect = e-116
 Identities = 202/350 (57%), Positives = 256/350 (73%), Gaps = 7/350 (2%)

Query: 5   NNPWDTTPAADSAAQSADAWGTPTTAPTDGGG--ADWLTSTPAPNVEH--FNILDPFHKT 60
           NNPW+T    +    +++ WG+  T PT+     ADWLT   A +     F+  DPF + 
Sbjct: 4   NNPWETPSQPEP---TSNPWGSAETIPTESISPQADWLTQAGAVDNTQTAFSWTDPFAQK 60

Query: 61  LIPLDSWVTEGIDWVVTHFRPVFQGVRVPVDYILNGFQQLLLGMPAPVAIIVFALIAWQI 120
           LIPLD WV  G+DW+V +FR VFQ +R+PVD IL   Q  LL +     ++ F L AWQI
Sbjct: 61  LIPLDHWVENGLDWLVDNFRDVFQAIRIPVDVILTALQTFLLSLNPWFVLVFFTLFAWQI 120

Query: 121 SGVGMGVATLVSLIAIGAIGAWSQAMVTLALVLTALLFCIVIGLPLGIWLARSPRAAKII 180
            G  +G+ +  SL+ IG +GAW + MVTLALV TA+LF +++G+PLGIW+ +S R   I 
Sbjct: 121 GGRKLGILSAASLLIIGFLGAWPETMVTLALVFTAVLFSMLVGIPLGIWMGKSNRMQSIF 180

Query: 181 RPLLDAMQTTPAFVYLVPIVMLFGIGNVPGVVVTIIFALPPIIRLTILGINQVPADLIEA 240
            P+LDAMQTTPAFVYL+PIVMLFGIGNVPGVVVTIIF+LPP++RLT LGI QVPADLIEA
Sbjct: 181 MPILDAMQTTPAFVYLIPIVMLFGIGNVPGVVVTIIFSLPPLVRLTSLGIRQVPADLIEA 240

Query: 241 SRSFGASPRQMLFKVQLPLAMPTIMAGVNQTLMLALSMVVIASMIAVGGLGQMVLRGIGR 300
             ++GA P QMLFK++LP+A  TIMAG+NQ LML+LSMVVIASMIAVGGLGQMVLRGIGR
Sbjct: 241 GHAYGAHPLQMLFKIELPVAKATIMAGINQNLMLSLSMVVIASMIAVGGLGQMVLRGIGR 300

Query: 301 LDMGLATVGGVGIVILAIILDRLTQAVGRDSRSRGNRRWYTTGPVGLLTR 350
           LDMGLA +GG+ IV+LAI+LDR+TQ++G+  +S     WY   P+  L +
Sbjct: 301 LDMGLAAIGGLSIVLLAIMLDRITQSMGQQPKSNTRIHWYQREPLWWLLK 350


Lambda     K      H
   0.326    0.141    0.435 

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: 420
Number of extensions: 14
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: 354
Length of database: 359
Length adjustment: 29
Effective length of query: 325
Effective length of database: 330
Effective search space:   107250
Effective search space used:   107250
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.0 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.6 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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