GapMind for catabolism of small carbon sources

 

Alignments for a candidate for malK_Aa in Skermanella stibiiresistens SB22

Align ABC-type maltose transporter (EC 7.5.2.1) (characterized)
to candidate WP_037454711.1 N825_RS16865 sn-glycerol-3-phosphate ABC transporter ATP-binding protein UgpC

Query= BRENDA::Q70HW1
         (384 letters)



>NCBI__GCF_000576635.1:WP_037454711.1
          Length = 362

 Score =  329 bits (844), Expect = 7e-95
 Identities = 185/363 (50%), Positives = 233/363 (64%), Gaps = 7/363 (1%)

Query: 1   MARVLLEHIYKTYPGQTEPTVKDFNLDIQDKEFTVFVGPSGCGKTTTLRMIAGLEDITEG 60
           MA V +  + K Y GQ E  +   +++I+D+EF V VGPSGCGK+T LRM+AGLE IT G
Sbjct: 1   MASVGIAQVRKAY-GQHE-VIHGIDIEIEDEEFVVLVGPSGCGKSTLLRMVAGLEQITGG 58

Query: 61  NLYIGDRRVNDVPPKDRDIAMVFQNYALYPHMTVYQNMAFGLKLRKVPKAEIDRRVQEAA 120
            + IG   VN VPPK+RDIAMVFQNYALYPHMTV+ NMAF L+LRK     + +RV+EAA
Sbjct: 59  EIAIGGTVVNLVPPKERDIAMVFQNYALYPHMTVFNNMAFSLQLRKSDPDMVQKRVREAA 118

Query: 121 KILDIAHLLDRKPKALSGGQRQRVALGRAIVREPQVFLMDEPLSNLDAKLRVQMRAEIRK 180
            IL +   LDR P+ LSGGQRQRVA+GRAIVR+PQVFL DEPLSNLDAKLRVQMR EI+ 
Sbjct: 119 DILGLVPYLDRYPRQLSGGQRQRVAMGRAIVRDPQVFLFDEPLSNLDAKLRVQMRTEIKA 178

Query: 181 LHQRLQTTVIYVTHDQTEAMTMGDRIVVMRDGVIQQADTPQVVYSQPKNMFVAGFIGSPA 240
           LHQRL+TT IYVTHDQ EAMTM DRIVVM DG ++Q  TP  +Y  P N FVAGFIGSP+
Sbjct: 179 LHQRLRTTSIYVTHDQVEAMTMADRIVVMHDGHVEQIGTPLELYDYPANTFVAGFIGSPS 238

Query: 241 MNFIRGEIVQDGDAFYFRAPSISLRLPEGRYGVLKASGAIGKPVVLGVRPEDLHDEEVFM 300
           MNF  G   +DG A +       +R P     + +A+   G+ V  G+RP  L       
Sbjct: 239 MNFFNGTFRRDGRAAWVEVAG-DIRFPV--EPLTRAND--GQSVTYGIRPGHLTLVNGDA 293

Query: 301 TTYPDSVLQMQVEVVEHMGSEVYLHTSIGPNTIVARVNPRHVYHVGSSVKLAIDLNKIHI 360
                  +   ++V+E  G +  +   +      A    RH +  G ++ L   +   H+
Sbjct: 294 APGFPKGVAATIQVIEPTGDDTVVFCRMANQEACAMFVERHAFRPGDTIMLMPRMANGHV 353

Query: 361 FDA 363
           FD+
Sbjct: 354 FDS 356


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: 423
Number of extensions: 21
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: 362
Length adjustment: 30
Effective length of query: 354
Effective length of database: 332
Effective search space:   117528
Effective search space used:   117528
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: 50 (23.9 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