Align putrescine-pyruvate transaminase (EC 2.6.1.113) (characterized)
to candidate 8499751 DvMF_0516 aminotransferase class-III (RefSeq)
Query= BRENDA::Q9I6J2 (456 letters) >lcl|FitnessBrowser__Miya:8499751 DvMF_0516 aminotransferase class-III (RefSeq) Length = 459 Score = 226 bits (577), Expect = 9e-64 Identities = 143/440 (32%), Positives = 220/440 (50%), Gaps = 19/440 (4%) Query: 20 HHLPPFTDYKQLNEKGARIITKAEGVYIWDSEGNKILDAMAG-LWCVNVGYGREELVQAA 78 HHL ++ KG I+ + EG+ + D G + LDA +G +WCVNVGYGRE + +A Sbjct: 22 HHL---VQHQAFAGKGPMIVVEGEGLTLRDINGKEYLDATSGGVWCVNVGYGRERIARAV 78 Query: 79 TRQMRELPFYNLFFQTAHPPVVELAKAIADVAPEGMNHVFFTGSGSEANDTVLRMVRHYW 138 QM+ +P+Y + P +E A+ + P G+ + + SGSEAN+ +MVR Sbjct: 79 YEQMKAMPYYAA--TAGNIPYIEFAQKLLAHMP-GLTRAYLSNSGSEANEKAYKMVRSLA 135 Query: 139 ATKGQPQKKVVIGRWNGYHGSTVAGVSLGGMKALHEQGDFPIPGIVHIAQPYWYGEGGDM 198 G P KK ++ R YHG+T+ +S G E +PG V Y + Sbjct: 136 HLSGNPAKKKILFRARDYHGTTLGALSSTGQAERKEWFGPLVPGFVEFPHACCYRCAFNK 195 Query: 199 SPDEFGVWAAEQLEKKILEVGEENVAAFIAEPIQGAGGVIVPPDTYWPKIREILAKYDIL 258 + + A +E+ I + G E V I EPI GGVI P Y+ + +I ++ +L Sbjct: 196 TYPGCDIDCARAVERIIEQEGPETVGGLIVEPITAGGGVIPPVAEYYTVLADICRRHGVL 255 Query: 259 FIADEVICGFGRTGEWFGSQYYGNAPDLMPIAKGLTSGYIPMGGVVVRDEIVEV-LNQGG 317 I DEV+CG GRTG FG Q+YG PD++ +AKG+ S Y+P+ +E+ + LN Sbjct: 256 LIMDEVVCGMGRTGTMFGYQHYGVTPDIVTMAKGVASAYMPISVTATTEEVFKAFLNDPA 315 Query: 318 E----FYHGFTYSGHPVAAAVALENIRILREEKIIEKVKAETAPYLQKRWQELADHPLVG 373 + F TY G + ALEN+ I+ EEK+++ V A YL +EL D P VG Sbjct: 316 DKMAYFRDISTYGGCAAGCSAALENMAIIEEEKLLDNVNA-MGDYLLAGLKELGDLPYVG 374 Query: 374 EARGVGMVAALELVKNKKTRERFTDKGVGMLCREHCFRNGLIMR------AVGDTMIISP 427 + RG G++ +ELV++K ++ + V + E L+ R + + I+P Sbjct: 375 DVRGKGLLCGIELVQDKAGKKPMAEGKVIQVVGEMAANAVLVGRTNRSLPGFNNIINIAP 434 Query: 428 PLVIDPSQIDELITLARKCL 447 V+ ID ++ R L Sbjct: 435 AYVVTRDNIDVILRTLRAAL 454 Lambda K H 0.320 0.138 0.425 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: 563 Number of extensions: 35 Number of successful extensions: 5 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: 456 Length of database: 459 Length adjustment: 33 Effective length of query: 423 Effective length of database: 426 Effective search space: 180198 Effective search space used: 180198 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: 51 (24.3 bits)
This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.
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:
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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.
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