GapMind for catabolism of small carbon sources

 

Alignments for a candidate for malK_Aa in Halomonas xinjiangensis TRM 0175

Align ABC-type maltose transporter (EC 7.5.2.1) (characterized)
to candidate WP_043527041.1 JH15_RS03500 sn-glycerol-3-phosphate import ATP-binding protein UgpC

Query= BRENDA::Q70HW1
         (384 letters)



>NCBI__GCF_000759345.1:WP_043527041.1
          Length = 354

 Score =  323 bits (828), Expect = 5e-93
 Identities = 187/367 (50%), Positives = 239/367 (65%), Gaps = 30/367 (8%)

Query: 1   MARVLLEHIYKTYPGQTEPTVKDFNLDIQDKEFTVFVGPSGCGKTTTLRMIAGLEDITEG 60
           MA + L  + KTY G  E  VK  +L+I D EF V VGPSGCGK+T LRM+AGLE IT+G
Sbjct: 1   MASIQLTGLKKTYAGNVE-AVKGIDLEIADGEFVVLVGPSGCGKSTLLRMVAGLETITDG 59

Query: 61  NLYIGDRRVNDVPPKDRDIAMVFQNYALYPHMTVYQNMAFGLKLRKVPKAEIDRRVQEAA 120
            L I DR VND+ P +RDIAMVFQNYALYPHMTV+ N+A+GLK R V + EI+RRV +AA
Sbjct: 60  TLKIDDRVVNDLEPAERDIAMVFQNYALYPHMTVFGNLAYGLKNRGVKREEIERRVHDAA 119

Query: 121 KILDIAHLLDRKPKALSGGQRQRVALGRAIVREPQVFLMDEPLSNLDAKLRVQMRAEIRK 180
            +L+I   L+RKP+ LSGGQRQRVA+GRA+VREP  FL DEPLSNLDAKLRVQMR EI++
Sbjct: 120 AMLEIEPFLERKPRKLSGGQRQRVAMGRALVREPSAFLFDEPLSNLDAKLRVQMRVEIKQ 179

Query: 181 LHQRLQTTVIYVTHDQTEAMTMGDRIVVMRDGVIQQADTPQVVYSQPKNMFVAGFIGSPA 240
           L +RL+TT +YVTHDQ EA+T+GDR+VV+  G I+Q  TP  VY +P +MFVA FIGSPA
Sbjct: 180 LQRRLKTTSLYVTHDQLEALTLGDRLVVLNGGSIEQVGTPMEVYEKPASMFVATFIGSPA 239

Query: 241 MNFIRGEIVQDGDAFYFRAPSISLRLPEGRYGVLKASGAIGKPVVLGVRPEDLHDEEVFM 300
           MN +               P   LR   G  G+L    A     V+G+RP+DL  E    
Sbjct: 240 MNML---------------PVAYLR-ERGANGLLDHLAA--DTDVIGIRPDDLRIEA--- 278

Query: 301 TTYPDS---VLQMQVEVVEHMGSEVYLHTSI--GPNTIVARVNPRHVYHVGSSVKLAIDL 355
              PD    V+   VE+ E  G+E +L+ S+       V R + R     G +++  +  
Sbjct: 279 ---PDEDHLVVTGTVELFEAAGAESHLYVSLEGSDQPTVIRTSARPPVAEGETMRFHVLP 335

Query: 356 NKIHIFD 362
           + +H F+
Sbjct: 336 SALHPFN 342


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: 402
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: 384
Length of database: 354
Length adjustment: 30
Effective length of query: 354
Effective length of database: 324
Effective search space:   114696
Effective search space used:   114696
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