GapMind for catabolism of small carbon sources

 

Alignments for a candidate for malK_Aa in Rhodobacter viridis JA737

Align ABC-type maltose transporter (EC 7.5.2.1) (characterized)
to candidate WP_110804036.1 C8J30_RS01990 sn-glycerol-3-phosphate ABC transporter ATP-binding protein UgpC

Query= BRENDA::Q70HW1
         (384 letters)



>NCBI__GCF_003217355.1:WP_110804036.1
          Length = 361

 Score =  288 bits (738), Expect = 1e-82
 Identities = 177/369 (47%), Positives = 229/369 (62%), Gaps = 21/369 (5%)

Query: 1   MARVLLEHIYKTYPGQTEPTVKDFNLDIQDKEFTVFVGPSGCGKTTTLRMIAGLEDITEG 60
           MA + L  + K+Y G+ +  ++D NLDI+  E  VFVGPSGCGK+T LRMIAGLE I+ G
Sbjct: 1   MADLKLTRVGKSY-GEVD-VLRDINLDIKAGELIVFVGPSGCGKSTLLRMIAGLERISAG 58

Query: 61  NLYIGDRRVNDVPPKDRDIAMVFQNYALYPHMTVYQNMAFGLKLRKVPKAEIDRRVQEAA 120
            L I   RVND+PP  R IAMVFQ+YALYPHMTV QNM F LK+ K  + +ID+ V+ AA
Sbjct: 59  ELRIDGVRVNDMPPAQRGIAMVFQSYALYPHMTVRQNMEFALKIAKKTRQDIDKAVENAA 118

Query: 121 KILDIAHLLDRKPKALSGGQRQRVALGRAIVREPQVFLMDEPLSNLDAKLRVQMRAEIRK 180
           +IL +   LDR PKALSGGQRQRVA+GRAIVR+P+V+L DEPLSNLDA LRV  R EI +
Sbjct: 119 RILQLTPYLDRLPKALSGGQRQRVAIGRAIVRDPKVYLFDEPLSNLDAALRVATRIEIAQ 178

Query: 181 LHQRL-QTTVIYVTHDQTEAMTMGDRIVVMRDGVIQQADTPQVVYSQPKNMFVAGFIGSP 239
           L + + + T+IYVTHDQ EAMT+  RIVV+ +  I Q  TP  +Y +P+  FVA FIGSP
Sbjct: 179 LKEAMPERTMIYVTHDQVEAMTLASRIVVLANKGIAQVGTPLELYEKPETEFVAQFIGSP 238

Query: 240 AMNFIRGEIVQDGDAFYFRAPSISLRLPEG---RYGVLKASGAIGKPVVLGVRPEDLHDE 296
            MN + G I + G           + L +G   R  V  +   +G  V +GVRPEDL   
Sbjct: 239 QMNLLPGVIRETGAV-------TVVALDDGGTARSTVPTSPADLGLRVNIGVRPEDL--- 288

Query: 297 EVFMTTYPDSVLQMQVEVVEHMGSEVYLHTSIGPNT--IVARVNPRHVYHVGSSVKLAID 354
                     +    VE+VE +G    L+ +  P    +VA++   H     S+V L   
Sbjct: 289 ---TVITEGGLFTGVVEIVEALGEVTLLYFAAKPGEPHMVAKLPGIHAGLRHSTVGLTAA 345

Query: 355 LNKIHIFDA 363
             K+H+F A
Sbjct: 346 PEKVHLFHA 354


Lambda     K      H
   0.321    0.138    0.395 

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: 375
Number of extensions: 22
Number of successful extensions: 3
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: 384
Length of database: 361
Length adjustment: 30
Effective length of query: 354
Effective length of database: 331
Effective search space:   117174
Effective search space used:   117174
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