GapMind for catabolism of small carbon sources

 

Alignments for a candidate for malK_Aa in Methanosarcina acetivorans C2A

Align ABC-type maltose transporter (EC 7.5.2.1) (characterized)
to candidate WP_011021256.1 MA_RS06420 ABC transporter ATP-binding protein

Query= BRENDA::Q70HW1
         (384 letters)



>NCBI__GCF_000007345.1:WP_011021256.1
          Length = 377

 Score =  172 bits (437), Expect = 1e-47
 Identities = 116/372 (31%), Positives = 191/372 (51%), Gaps = 25/372 (6%)

Query: 7   EHIYKTYPGQTEPTVKDFNLDIQ---DKEFTVFVGPSGCGKTTTLRMIAGLEDITEGNLY 63
           +H  +    +   T K F LD+    D E  V  GPSG GKTT  + I+G+     G + 
Sbjct: 11  KHYTEAEINRKRSTGKAFTLDVSFEMDNELVVLFGPSGSGKTTLFKCISGITQPDNGKIT 70

Query: 64  IG-------DRRVNDVPPKDRDIAMVFQNYALYPHMTVYQNMAFGLKLRKVPKAEIDRRV 116
           +G       D+++N +P + R++  VFQNY L+PHM V +N+  GLK  K  K + + RV
Sbjct: 71  VGSKIYYDKDKKIN-LPIQKRNLGYVFQNYTLFPHMNVRKNIECGLK--KWEKEDREVRV 127

Query: 117 QEAAKILDIAHLLDRKPKALSGGQRQRVALGRAIVREPQVFLMDEPLSNLDAKLRVQMRA 176
            E   +L I  L  R P  +SGGQ+QRVAL RA+  +P + L+DEP S LD ++R ++  
Sbjct: 128 MEMLNLLHIEELETRYPSQISGGQKQRVALARALAPKPGILLLDEPFSALDMEIRTELAD 187

Query: 177 EIRKLHQRLQTTVIYVTHDQTEAMTMGDRIVVMRDGVIQQADTPQVVYSQPKNMFVAGFI 236
           +I+ L ++++  ++++TH+  EA  + DRI+++  G IQQ  TP+ ++ QP N+ V+  I
Sbjct: 188 KIKNLQKKIEIPLLFITHNLEEAFLLADRILILHGGKIQQFGTPEEIFYQPANLQVSELI 247

Query: 237 GSPAMNFIRGEIVQDGDAFYFRAPSISLRLPEGRYGVLKASGAIGKPVVLGVRPEDLHDE 296
           G    N      V++ D     + S  LR  + R  +   +   G  V  G+ PE++   
Sbjct: 248 G--ISNIFDDAYVEEYDK---ESKSTVLRSGDMRIKIESPNFKAGDKVTWGIYPENITLL 302

Query: 297 EVFMTTYPD-SVLQMQVEVVEHMG--SEVYLHTSIGPNTIVARVNPRHV----YHVGSSV 349
            V  +   D ++    V  + + G    + L       T++A V  + V     H G   
Sbjct: 303 PVSGSEDQDENIYSAHVNNIINKGPKKRITLKLVRYNKTLIAEVPAQFVDSLELHAGGFC 362

Query: 350 KLAIDLNKIHIF 361
            + +++NK+  F
Sbjct: 363 LVRLEMNKVVAF 374


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: 331
Number of extensions: 19
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: 377
Length adjustment: 30
Effective length of query: 354
Effective length of database: 347
Effective search space:   122838
Effective search space used:   122838
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 Apr 09 2024. 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