GapMind for catabolism of small carbon sources

 

Alignments for a candidate for malK_Aa in Tistlia consotensis USBA 355

Align ABC-type maltose transporter (EC 7.5.2.1) (characterized)
to candidate WP_085123761.1 B9O00_RS16330 ABC transporter ATP-binding protein

Query= BRENDA::Q70HW1
         (384 letters)



>NCBI__GCF_900177295.1:WP_085123761.1
          Length = 361

 Score =  323 bits (829), Expect = 4e-93
 Identities = 185/374 (49%), Positives = 242/374 (64%), Gaps = 20/374 (5%)

Query: 1   MARVLLEHIYKTYPGQTEPTVKDFNLDIQDKEFTVFVGPSGCGKTTTLRMIAGLEDITEG 60
           M  V  +H++K + G     ++DF+L++ D EF  F+GPSGCGKTTTLRM AGLE  T G
Sbjct: 1   MVSVRYQHLHKAF-GDGSVALQDFSLEVADGEFLTFLGPSGCGKTTTLRMTAGLETPTSG 59

Query: 61  NLYIGDRRVNDVPPKDRDIAMVFQNYALYPHMTVYQNMAFGLKLRKVPKAEIDRRVQEAA 120
            ++ G+R V D+PP  R+IAMVFQ+YALYPHMTV QN+ + L+ + V + E  RR    A
Sbjct: 60  EIFFGERPVVDLPPGRRNIAMVFQSYALYPHMTVQQNLEYPLRKQGVARDERARRATALA 119

Query: 121 KILDIAHLLDRKPKALSGGQRQRVALGRAIVREPQVFLMDEPLSNLDAKLRVQMRAEIRK 180
             L +  LL R+PK LSGGQ+QRVALGRA++REP+VFL+DEPLSNLDA+LR QMRAE+ +
Sbjct: 120 ATLQLDALLHRRPKHLSGGQQQRVALGRALIREPEVFLLDEPLSNLDAELRTQMRAELIQ 179

Query: 181 LHQRLQTTVIYVTHDQTEAMTMGDRIVVMRDGVIQQADTPQVVYSQPKNMFVAGFIGSPA 240
           LH+R+  T+IYVTHDQ EAMTM  RI VM  G +QQ  TP  +Y +P+N FVA F+GSPA
Sbjct: 180 LHRRIGRTMIYVTHDQVEAMTMSTRIAVMSKGELQQVGTPLEIYREPRNRFVAAFVGSPA 239

Query: 241 MNFIRGEI-VQDGDAFYFRAPSISLRLPEGR----YGVLKASGAIGKPVVLGVRPEDLHD 295
           MNF+ G I ++DG A  FRA  + + LP+ R     G+ +ASG     V+ G+RPE L  
Sbjct: 240 MNFVEGGIELRDGRA-VFRAAGLEVALPDARSARLAGLARASG-----VLAGIRPEHLSL 293

Query: 296 EEVFMTTYPDSVLQMQVEVVEHMGSEVYLHTSIGPNTIVARVNPRHVYHVGSSVKLAIDL 355
           E       P S  + +V VVE MG E  +        IV R         G  V L +D 
Sbjct: 294 E-------PGSG-EGRVLVVEAMGHEDIVTAETPAGRIVVRSAGTATAAAGDLVPLRVDP 345

Query: 356 NKIHIFDAETEESI 369
            K+H+FDA + E +
Sbjct: 346 EKLHLFDAASGERL 359


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: 17
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: 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 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